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27034-77-1

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27034-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27034-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,3 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27034-77:
(7*2)+(6*7)+(5*0)+(4*3)+(3*4)+(2*7)+(1*7)=101
101 % 10 = 1
So 27034-77-1 is a valid CAS Registry Number.

27034-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzoylimidazolidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Imidazolidinone,1-benzoyl

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:27034-77-1 SDS

27034-77-1Relevant articles and documents

Direct N-acylation of lactams, oxazolidinones, and imidazolidinones with aldehydes by Shvo's catalyst

Zhang, Jian,Hong, Soon Hyeok

supporting information, p. 4646 - 4649 (2012/10/29)

Direct N-acylation of lactams, oxazolidinones, and imidazolidinones was achieved with aldehydes by Shvo's catalyst without using any other stoichiometric reagent. The N-acylations with α,β-unsaturated aldehydes were achieved with excellent yields.

A novel and efficient reaction of imidazolidin-2-one and N-acylbenzotriazoles: A facile synthesis of 1-acylimidazolidin-2-one

Li, Jianjun,Sun, Yan,Chen, Zhiwei,Su, Weike

experimental part, p. 3669 - 3677 (2011/02/23)

Acylation of imidazolidin-2-one with readily available N- acylbenzotriazoles, in the presence of K2CO3, produced 1-acylimidazolidin-2-ones and N,N'-diacyl-imidazolidin-2-one in moderate to good yields. The utilization of N-acylbenzotriazoles which make the reaction simple and mild, may be especially advantageous when the corresponding acid chlorides are not stable or not easily prepared. It's also an example of the reaction of N-acylbenzotriazoles and amide. Copyright

Synthesis of 3-alkyl-2-benzamido-4-hydroxybut-2-enoic acid γ-lactones from alkyl cuprates. Attempted transformation to 2,3-diamino carboxylic acids by hydrogenation and Curtius rearrangement

Olsen,Hennen,Wardle

, p. 4605 - 4611 (2007/10/02)

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