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112077-92-6

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112077-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112077-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,7 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112077-92:
(8*1)+(7*1)+(6*2)+(5*0)+(4*7)+(3*7)+(2*9)+(1*2)=96
96 % 10 = 6
So 112077-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO3/c1-8-6-4-5-7-11(8)12(9(2)13)15-10(3)14/h4-7H,1-3H3

112077-92-6SDS

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 (N-acetyl-2-methylanilino) acetate

1.2 Other means of identification

Product number -
Other names N-(acetyloxy)-N-(2-methylphenyl)acetamide

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:112077-92-6 SDS

112077-92-6Downstream Products

112077-92-6Relevant articles and documents

Catalyst-free generation of acyl radicals induced by visible light in water to construct C-N bonds

Ran, Maogang,He, Jiaxin,Yan, Boyu,Liu, Wenbo,Li, Yi,Fu, Yunfen,Li, Chao-Jun,Yao, Qiuli

, p. 1970 - 1975 (2021/03/16)

We describe herein a catalyst-free and redox-neutral photochemical strategy for the direct generation of acyl radicals from α-diketones, and its selective conversion of nitrosoarenes to hydroxyamides or amides with AcOH or NaCl as an additive. The reaction was carried out under mild conditions in water with purple LEDs as the light source. A broad scope of substrates was demonstrated. Mechanistic experiments indicate that α-diketones cleave to give acyl radicals, with hydroxyamides being further reduced to amides.

A novel one pot reductive acetylation of nitroarenes

Baruah

, p. 300 - 303 (2007/10/03)

Nitroarenes are reductively acetylated in one pot to the corres, ponding N-arylacetamides and N-(acetyloxy)-N-arylacetamides with Zn and Ac2O in presence of acidic Al2O3 in dichloromethane at room temperature.

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