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29111-73-7

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  • Carbamic acid,(4-methyl-2-nitrophenyl)-, methyl ester (9CI)

    Cas No: 29111-73-7

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29111-73-7 Usage

General Description

4-(N-Acetyl)amino-3-nitrotoluene is a chemical compound known for its use in the production of dyes and pigments. It is characterized by its orange crystalline appearance and low solubility in water. It is often used as an intermediate substance in various chemical reactions and processes. This chemical compound has high stability and good heat resistance that adds to its widely used industrial applications. Due to its potentially toxic and harmful impacts, the handling and usage of 4-(N-Acetyl)amino-3-Nitrotoluene must follow strict safety measures and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 29111-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,1 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29111-73:
(7*2)+(6*9)+(5*1)+(4*1)+(3*1)+(2*7)+(1*3)=97
97 % 10 = 7
So 29111-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O4/c1-6-3-4-7(10-9(12)15-2)8(5-6)11(13)14/h3-5H,1-2H3,(H,10,12)

29111-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(N-ACETYL)AMINO-3-NITROTOLUENE

1.2 Other means of identification

Product number -
Other names Methyl-N-(4-methyl-2-nitrophenyl)carbamat

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:29111-73-7 SDS

29111-73-7Relevant articles and documents

The first intramolecular Heck-Matsuda reaction and its application in the syntheses of benzofurans and indoles

Siqueira, Fernanda A.,Taylor, Jason G.,Correia, Carlos Roque D.

supporting information; experimental part, p. 2102 - 2105 (2010/06/14)

In this Letter, we report, for the first time, the development of an efficient method for the intramolecular Heck reaction of arenediazonium salts in the synthesis of benzofuran and indole derivatives. In addition, this methodology allowed the synthesis of a series of dihydrobenzofuran acetic acid derivatives via a domino Heck-Matsuda coupling-carbonylation reaction.

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