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2-acetamido-4-methylphenyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75813-74-0

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75813-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75813-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,1 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75813-74:
(7*7)+(6*5)+(5*8)+(4*1)+(3*3)+(2*7)+(1*4)=150
150 % 10 = 0
So 75813-74-0 is a valid CAS Registry Number.

75813-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetamido-4-methylphenyl acetate

1.2 Other means of identification

Product number -
Other names diacetyl-2-amino-4-methylphenol

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:75813-74-0 SDS

75813-74-0Downstream Products

75813-74-0Relevant academic research and scientific papers

Palladium-catalyzed C-H activation of anilides at room temperature: Ortho-arylation and acetoxylation

Yang, Fan,Song, Feijie,Li, Wei,Lan, Jingbo,You, Jingsong

, p. 9649 - 9652 (2013/09/02)

Room-temperature ortho-arylation and acetoxylation of anilides have been achieved using cationic palladium (Pd[TFA]+) as catalyst and (NH 4)2S2O8 as oxidant. Preliminary investigation of the mechanism

Direct ortho-acetoxylation of anilides via palladium-catalyzed sp 2 C-H bond oxidative activation

Wang, Guan-Wu,Yuan, Ting-Ting,Wu, Xue-Liang

, p. 4717 - 4720 (2008/09/21)

(Chemical Equation Presented) Various anilides have been directly ortho-acetoxylated through a Pd(OAc)2-catalyzed C-H bond activation process. The amide group in anilides was found to functionalize as an elegant directing group to convert aromatic sp2 C-H bonds into C-O bonds in high regioselectivity with acetic acid as the acetate source and K 2S2O8 as the oxidant.

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