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5832-44-0

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5832-44-0 Usage

Chemical Properties

Deliquescent cryst

Uses

Different sources of media describe the Uses of 5832-44-0 differently. You can refer to the following data:
1. 4-Methyl-3-nitropyridine may be used as a starting material in the synthesis of ethyl 6-azaindole-2-carboxylate and also 3-substituted azaindoles.
2. 4-METHYL-3-NITROPYRIDINE is a useful research chemical.

General Description

4-Methyl-3-nitropyridine, a substituted nitropyridine, can be prepared by the malonation of 4-methoxy-3-nitropyridine with sodium diethyl malonate.

Check Digit Verification of cas no

The CAS Registry Mumber 5832-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5832-44:
(6*5)+(5*8)+(4*3)+(3*2)+(2*4)+(1*4)=100
100 % 10 = 0
So 5832-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c1-5-2-3-7-4-6(5)8(9)10/h2-4H,1H3

5832-44-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L07398)  4-Methyl-3-nitropyridine, 98%   

  • 5832-44-0

  • 1g

  • 594.0CNY

  • Detail
  • Alfa Aesar

  • (L07398)  4-Methyl-3-nitropyridine, 98%   

  • 5832-44-0

  • 5g

  • 2525.0CNY

  • Detail
  • Aldrich

  • (532592)  4-Methyl-3-nitropyridine  97%

  • 5832-44-0

  • 532592-1G

  • 686.79CNY

  • Detail
  • Aldrich

  • (532592)  4-Methyl-3-nitropyridine  97%

  • 5832-44-0

  • 532592-5G

  • 2,416.05CNY

  • Detail

5832-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-3-nitropyridine

1.2 Other means of identification

Product number -
Other names Methyl-3-nitropyridine,4

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:5832-44-0 SDS

5832-44-0Relevant articles and documents

Selective ortho methylation of nitroheteroaryls by vicarious nucleophilic substitution

Achmatowicz, Michal,Thiel, Oliver R.,Gorins, Gilles,Goldstein, Corinne,Affouard, Caroline,Jensen, Randy,Larsen, Robert D.

, p. 6793 - 6799 (2008/12/22)

(Chemical Equation Presented) An efficient and scalable three-step one-pot approach to 6-methyl-5-nitroisoquinoline (1) from inexpensive 5-nitroisoquinoline, utilizing the vicarious nucleophilic substitution (VNS) as a key step, is described. The optimized reaction conditions can be applied to a limited number of other aromatic and heteroaromatic nitro compounds. Attempts to understand the observed selectivity in the VNS step led to the discovery of two new reaction pathways under VNS conditions, one leading to an isoxazole and the other resulting in the formal cyclopropanation of an aromatic nitro compound.

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