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24501-21-1

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24501-21-1 Usage

General Description

2,4-diamino-3-(nitro)pyridine is an organic compound with the chemical formula C5H6N4O2. It consists of a pyridine ring with amino groups at the 2 and 4 positions, and a nitro group at the 3 position. 2,4-diamino-3-(nitro)pyridine is commonly used in the synthesis of pharmaceuticals and agrochemicals, as well as in the manufacture of dyes and pigments. It is also used as a building block in organic chemistry, and its derivatives have shown potential in the treatment of certain diseases. 2,4-diamino-3-(nitro)pyridine is a versatile chemical that holds promise in a variety of applications due to its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 24501-21-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,0 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24501-21:
(7*2)+(6*4)+(5*5)+(4*0)+(3*1)+(2*2)+(1*1)=71
71 % 10 = 1
So 24501-21-1 is a valid CAS Registry Number.

24501-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitropyridine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 3-nitro-pyridine-2,4-diyldiamine

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:24501-21-1 SDS

24501-21-1Relevant articles and documents

Process Development and Multikilogram-Scale Synthesis of a TRPV1 Antagonist

Cleator, Ed,Scott, Jeremy P.,Avalle, Paulo,Bio, Matthew M.,Brewer, Sarah E.,Davies, Antony J.,Gibb, Andrew D.,Sheen, Faye J.,Stewart, Gavin W.,Wallace, Debra J.,Wilson., Robert D.

, p. 1561 - 1567 (2014/01/06)

The process development and multikilogram preparation of a TRPV1 antagonist, 1, is described. Pyrido[2,3-b]pyrazine 1 was prepared in a convergent manner by the coupling of two key fragments, glyoxal 2 and diamine 3. Glyoxal 2 was synthesized in six chemical steps in 20% overall yield, the key step being a challenging Grignard reaction to install the glyoxalate moiety. Diamine 3 was also prepared in six chemical steps in 46% overall yield, exploiting a regioselective nucleophilic aromatic substitution to obtain the key nitrodiamine intermediate 19.

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