109613-90-3

• 

• Basic information

  1. Product Name: 2-CHLORO-3-FLUORO-4-NITROPYRIDINE
  2. Synonyms: 2-CHLORO-3-FLUORO-4-NITROPYRIDINE
  3. CAS NO:109613-90-3
  4. Molecular Formula: C5H2ClFN2O2
  5. Molecular Weight: 176.5329832
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 109613-90-3.mol

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
  8. Solubility: N/A
  9. CAS DataBase Reference: 2-CHLORO-3-FLUORO-4-NITROPYRIDINE(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2-CHLORO-3-FLUORO-4-NITROPYRIDINE(109613-90-3)
  11. EPA Substance Registry System: 2-CHLORO-3-FLUORO-4-NITROPYRIDINE(109613-90-3)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 109613-90-3(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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109613-90-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-3-fluoro-4-nitropyridine is used as a key intermediate in the synthesis of various drugs and pharmaceuticals. Its unique chemical structure allows for the development of new therapeutic agents with specific properties and functions.
Used in Agrochemical Industry:
In the agrochemical industry, 2-chloro-3-fluoro-4-nitropyridine serves as a building block for the manufacturing of various agrochemicals. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases in agriculture.
Used in Organic Synthesis:
2-Chloro-3-fluoro-4-nitropyridine is also utilized as a versatile building block in organic synthesis. Its presence in various chemical reactions can lead to the formation of new compounds with diverse applications in different fields.
Safety Precautions:
Due to its potentially hazardous nature, 2-chloro-3-fluoro-4-nitropyridine should be handled and stored with proper care. Adequate safety measures, such as wearing protective gear and following established protocols, must be taken to minimize the risk of exposure and ensure the safety of individuals working with 2-CHLORO-3-FLUORO-4-NITROPYRIDINE.

Check Digit Verification of cas no

The CAS Registry Mumber 109613-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,6,1 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109613-90:
(8*1)+(7*0)+(6*9)+(5*6)+(4*1)+(3*3)+(2*9)+(1*0)=123
123 % 10 = 3
So 109613-90-3 is a valid CAS Registry Number.

109613-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-Chloro-3-fluoro-4-nitropyridine

1.2 Other means of identification

Product number	-
Other names	Pyridine,2-chloro-3-fluoro-4-nitro

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:109613-90-3 SDS

109613-90-3Upstream product

• 85386-94-3 2-Chlor-3-fluorpyridin-1-oxid 
• 17282-04-1 2-chloro-3-fluoropyridine 
• 101664-56-6 2-Chlor-3-fluor-4-nitropyridin-1-oxid 

109613-90-3Downstream Products

• 128702-03-4 2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-8-amine 

109613-90-3Relevant articles and documents

Syntheses of Hydroxylated Bipyridines, I. - Orellanine, the Poison of a Toadstool

Dehmlow, Eckehard V.,Schulz, Hans-Joachim

, p. 857 - 862 (2007/10/02)

Two syntheses of orellanine, -3,3',4,4'-tetrol-1,1'-dioxide (5b), are developed which comprise 10 or 11 steps, respectively.The chemical reactions of 5b with diazomethane and on UV irradiation are described.

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