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127082-54-6

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127082-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127082-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,8 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127082-54:
(8*1)+(7*2)+(6*7)+(5*0)+(4*8)+(3*2)+(2*5)+(1*4)=116
116 % 10 = 6
So 127082-54-6 is a valid CAS Registry Number.

127082-54-6SDS

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 2-Benzamido-N-methylbenzamide

1.2 Other means of identification

Product number -
Other names N-Benzoyl-anthranilsaeure-methylamid

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:127082-54-6 SDS

127082-54-6Relevant articles and documents

[Cp*RhIII]/Ionic Liquid as a Highly Efficient and Recyclable Catalytic Medium for C?H Amidation

Ma, Qiang,Yu, Xinling,Lai, Ruizhi,Lv, Songyang,Dai, Weiyang,Zhang, Chen,Wang, Xiaolong,Wang, Qiantao,Wu, Yong

, p. 3672 - 3678 (2018/09/29)

A [Cp*RhIII]-catalyzed direct C?H amidation is carried out in ionic liquid. Both C(sp2)?H bonds of (hetero)arenes and alkenes and unactivated C(sp3)?H bonds can be easily amidated with high functional-group tolerance and excellent yields under these conditions. Notably, using [Cp*RhIII]/[BMIM]BF4 (BMIM=1-butyl-3-methylimidazolium) as the green and recyclable medium is environmentally benign, in light of characteristics such as the reusability of the expensive rhodium catalyst, avoidance of highly toxic organic solvents, and mild reaction conditions, as well as a short reaction time.

Mechanism of alkaline cyclization of 2-(substituted benzamido)benzamides to 4-quinazolinones

Gardner,Kanagasooriam,Smyth,Williams

, p. 6245 - 6250 (2007/10/02)

The title amides cyclize rapidly to the corresponding quinazolin-4-ones in aqueous alkaline solution at 25°C; the pseudo-first-order rate constants fit the empirical equation k(obs) = k(max) [OH-]/(K(m) + [OH-] + [OH-]sup

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