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CAS

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3,5-Difluorobenzaldehyde is an organic compound with the chemical formula C7H4F2O. It is a clear light green liquid at room temperature and is characterized by its 19F′H spectra when studied in a low-temperature dimethyl ether solution.

32085-88-4

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32085-88-4 Usage

Uses

Used in Pharmaceutical Industry:
3,5-Difluorobenzaldehyde is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique chemical structure allows for the development of new drugs with potential therapeutic benefits.
Used in Chemical Synthesis:
3,5-Difluorobenzaldehyde is used as a building block in the chemical synthesis of various organic compounds, including fluorinated aromatics, for [application reason]. Its presence of two fluorine atoms provides distinct reactivity and properties compared to its non-fluorinated counterparts, making it a valuable component in the synthesis of specialty chemicals.
Used in Material Science:
3,5-Difluorobenzaldehyde is used as a precursor in the development of advanced materials, such as polymers and coatings, for [application reason]. The incorporation of fluorine atoms can enhance the material's properties, such as chemical resistance, thermal stability, and non-stick characteristics.
Used in Agrochemical Industry:
3,5-Difluorobenzaldehyde is used as a starting material in the production of agrochemicals, such as pesticides and herbicides, for [application reason]. Its unique chemical properties can contribute to the development of more effective and environmentally friendly products in the agricultural sector.

Synthesis Reference(s)

Journal of Medicinal Chemistry, 30, p. 486, 1987 DOI: 10.1021/jm00386a008

Check Digit Verification of cas no

The CAS Registry Mumber 32085-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,8 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32085-88:
(7*3)+(6*2)+(5*0)+(4*8)+(3*5)+(2*8)+(1*8)=104
104 % 10 = 4
So 32085-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H3F6NO2/c9-7(10,11)4-1-2-5(8(12,13)14)6(3-4)15(16)17/h1-3H

32085-88-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A16917)  3,5-Difluorobenzaldehyde, 97%   

  • 32085-88-4

  • 1g

  • 358.0CNY

  • Detail
  • Alfa Aesar

  • (A16917)  3,5-Difluorobenzaldehyde, 97%   

  • 32085-88-4

  • 5g

  • 1185.0CNY

  • Detail
  • Alfa Aesar

  • (A16917)  3,5-Difluorobenzaldehyde, 97%   

  • 32085-88-4

  • 25g

  • 4739.0CNY

  • Detail

32085-88-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Difluorobenzaldehyde

1.2 Other means of identification

Product number -
Other names 3,5-difluororobenzaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32085-88-4 SDS

32085-88-4Relevant articles and documents

Synthesis of new Zn (II) complexes for photo decomposition of organic dye pollutants, industrial wastewater and photo-oxidation of methyl arenes under visible-light

Ahemed, Jakeer,Bhongiri, Yadagiri,Chetti, Prabhakar,Gade, Ramesh,Kore, Ranjith,Pasha, Jakeer,Pola, Someshwar,Rao D, Venkateshwar

, (2021/07/28)

Synthesis of new Schiff's base Zn-complexes for photo-oxidation of methyl arenes and xylenes are reported under visible light irradiation conditions. All the synthesized new ligands and Zn-complexes are thoroughly characterized with various spectral analyses and confirmed as 1:1 ratio of Zn and ligand with distorted octahedral structure. The bandgap energies of the ligands are higher than its Zn-complexes. These synthesized new Zn(II) complexes are used for the photo-fragmentation of organic dye pollutants, photodegradation of food industrial wastewater and oxidation of methyl arenes which are converted into its respective aldehydes with moderate yields under visible light irradiation. The photooxidation reaction dependency on the intensity of the visible light was also studied. With the increase in the dosage of photocatalyst, the methyl groups are oxidized to get aldehydes and mono acid products, which are also identified from LC-MS data. Finally, [Zn(PPMHT)Cl] is with better efficiency than [Zn(PTHMT)Cl] and [Zn(MIMHPT)Cl] for oxidation of methyl arenes is reported under visible-light-driven conditions.

A one-pot synthesis of benzimidazoles via aerobic oxidative condensation of benzyl alcohols with o-phenylenediamines catalyzed by [MIMPs]+Cl-/NaNO2/TEMPO

Geng, Zhenzhen,Zhang, Hong-Yu,Yin, Guohui,Zhang, Yuecheng,Zhao, Jiquan

, p. 557 - 565 (2020/03/30)

The ionic liquid 1-methyl-3-(3-sulfopropyl)imidazolium chloride ([MIMPs]+Cl-) in combination with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) and sodium nitrite (NaNO2) as a catalytic system demonstrates high efficiency in the one-pot two-step aerobic oxidative condensation of benzyl alcohols with 1,2-phenylenediamines to give benzimidazoles. Various benzimidazoles are obtained in good to excellent yields by this strategy.

Aerobic oxidation of alcohols by copper(I)/benzoxazine ligand/TEMPO under mild and base-free conditions

Zhang,Huang,Lü,Cao,Zhao

, p. 1965 - 1972 (2015/10/12)

A novel benzoxazine ligand with an imidazole moiety was synthesized. This ligand in combination with Cu(OTf) and TEMPO efficiently catalyzed aerobic oxidation of active primary alcohols and also showed good to excellent activity in the oxidation of secondary alcohols under mild and base-free conditions.

Palladium-catalyzed synthesis of aldehydes from aryl halides and tert-butyl isocyanide using formate salts as hydride donors

Zhang, Ying,Jiang, Xiao,Wang, Jin-Mei,Chen, Jing-Lei,Zhu, Yong-Ming

, p. 17060 - 17063 (2015/03/30)

An efficient one-pot palladium-catalyzed hydroformylation of aryl halides to produce aromatic aldehydes has been achieved, employing tert-butyl isocyanide as a C1 resource and formate salt as a hydride donor without any additional bases. Characterized by its mild reaction conditions, easy operation and lower toxicity, this reaction can tolerate a wide array of functional groups with moderate to excellent yields.

Deep eutectic solvent supported TEMPO for oxidation of alcohols

Zhang, Yuecheng,Lü, Fenglian,Cao, Xiaohui,Zhao, Jiquan

, p. 40161 - 40169 (2015/02/03)

A novel deep eutectic solvent supported TEMPO (DES-TEMPO) composed of N,N-dimethyl-(4-(2,2,6,6-tetramethyl-1-oxyl-4-piperidoxyl)butyl)dodecyl ammonium salt ([Quaternium-TEMPO]+Br-) and urea was prepared. An efficient catalytic system for the oxidation of alcohols with molecular oxygen as terminal oxidant has been developed from DES-TEMPO and Fe(NO3)3·9H2O. The DES-TEMPO/Fe(NO3)3system showed good performances on the selective oxidation of various alcohols to the corresponding aldehydes and ketones under mild and solvent-free conditions. The DES could be recovered easily and recycled up to five times in the oxidation of benzyl alcohol without significant loss of catalytic activity. This journal is

Palladium-catalyzed formylation of aryl halides with tert -butyl isocyanide

Jiang, Xiao,Wang, Jin-Mei,Zhang, Ying,Chen, Zhong,Zhu, Yong-Ming,Ji, Shun-Jun

supporting information, p. 3492 - 3495 (2014/07/21)

A novel palladium-catalyzed formylation of aryl halides with isocyanide in the presence of Et3SiH has been demonstrated, which provides a strategy toward important aldehydes with moderate to excellent yield. The advantage of this reaction includes milder conditions, convenient operation, lower toxicity, and wide functional group tolerance.

Electrophilicities of symmetrically substituted 1,3-diarylallyl cations

Troshin, Konstantin,Schindele, Claus,Mayr, Herbert

experimental part, p. 9391 - 9408 (2012/01/06)

Kinetics of the reactions of nine symmetrically substituted 1,3-diarylallyl cations with different nucleophiles were studied photometrically in dichloromethane, acetonitrile, and DMSO solutions. The second-order rate constants k2 were found to follow the correlation log k2 = sN(N + E). The electrophilicity parameters E of the title cations were derived, using the known values of sN and N of the nucleophilic reaction partners, and compared with the electrophilicities of analogously substituted benzhydrylium ions. Good linear correlations were found between the electrophilicities E and the quantum chemically calculated gas-phase methyl anion affinities of the allyl cations and the σ+ constants of the substituents X.

Synthesis and mesomorphic properties of tolane-based fluorinated liquid crystals with an acrylate linkage

Chen, Ximin,Shen, Yuehai,Wen, Jianxun

experimental part, p. 138 - 146 (2011/05/12)

Six series of tolane-based fluorinated liquid crystals containing an acrylate linker were synthesized and their mesomorphic properties were characterized. The compounds generally exhibit SmA and N phases in wide temperature ranges. The introduction of acrylate linkers increases the clearing points by 20°C-30°C and suppresses the formation of higher ordered monotropic SmB phases. para-Fluorination is favorable for the mesophase stability, whereas meta-fluorination is not. The introduction of a 2,3,5,6-tetrafluorophenylene group decreases the clearing points and also suppresses the formation of the monotropic SmB phase. Copyright Taylor & Francis Group, LLC.

TEMPO/HCl/NaNO2 catalyst: A transition-metal-free approach to efficient aerobic oxidation of alcohols to aldehydes and ketones under mild conditions

Wang, Xinliang,Liu, Renhua,Jin, Yu,Liang, Xinmiao

supporting information; experimental part, p. 2679 - 2685 (2009/04/10)

Hydrochloric acid, a very inexpensive and readily available inorganic acid, has been found to cooperate exquisitely with NaNO2/TEMPO in catalyzing the molecular-oxygen-driven oxidation of a broad range of alcohol substrates to the corresponding aldehydes and ketones. This transition-metal- free catalytic oxidative conversion is novel and represents an interesting alternative route to the corresponding carbonyl compounds to the metal-catalyzed aerobic oxidation of alcohols.The reaction is highly selective with respect to the desired product when carried out at room temperature in air at atmospheric pressure. Notably, the use of very inexpensive NaNO2 and HCl in combination with TEMPO for this highly selective aerobic oxidation of alcohols in air at ambient temperaturemakes the reaction operationally and economically very attractive. The results of mechanistic studies, performed with the aid of electrospray ionization mass spectrometry (ESI-MS), are presented and discussed. TEMPO, TEMPOH, and TEMPO+ were observed in the redox cycle by means of ESI-MS. On the basis of these observations, a mechanism is proposed that may provide an insight into the newly developed aerobic alcohol oxidation.

Fluorine-substituted-4-alkenylbenzoic acid and derivatives thereof, and nematic liquid crystal composition containing cyanophenyl benzoate derivatives and liquid crystal display system using the same

-

, (2008/06/13)

A novel liquid crystal compound, a nematic liquid crystal composition, and a liquid crystal display system using the composition are disclosed herein. The liquid crystal compound is represented by the general formula (I): wherein R represents a hydrogen a

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