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2-Nitro-5-acetamido-4-methylbenzoic acid is a chemical compound with the molecular formula C10H10N2O5. It is a derivative of benzoic acid, featuring a nitro group at the 2-position, an acetamido group at the 5-position, and a methyl group at the 4-position. 2-NITRO-5-ACETYLAMINO-4-METHYLBENZOIC ACID is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds. It is an important intermediate in the production of certain drugs, particularly those with anti-inflammatory properties. The compound's structure and reactivity make it a valuable building block in organic chemistry, allowing for further functionalization and the creation of a variety of complex molecules.

6632-23-1

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6632-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6632-23-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6632-23:
(6*6)+(5*6)+(4*3)+(3*2)+(2*2)+(1*3)=91
91 % 10 = 1
So 6632-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O5/c1-5-3-9(12(16)17)7(10(14)15)4-8(5)11-6(2)13/h3-4H,1-2H3,(H,11,13)(H,14,15)

6632-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetamido-4-methyl-2-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 5-Acetamino-2-nitro-p-toluolsaeure

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 -
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More Details:6632-23-1 SDS

6632-23-1Downstream Products

6632-23-1Relevant academic research and scientific papers

The synthesis of C2-symmetric and axially chiral compounds for recognition and catalysis

Clews, John,Curtis, Anthony D.M.,Malkin, Hugh

, p. 8735 - 8746 (2007/10/03)

Axially chiral amidines and guanidines, some possessing C2-symmetry, have been targeted as potential chiral catalysts for reactions of α,β-unsaturated carboxylic acids or esters. The key step in each synthesis required the coupling of two sterically demanding aromatic compounds to form atropisomeric biaryl species. (C) 2000 Elsevier Science Ltd.

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