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105887-23-8

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105887-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105887-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,8 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105887-23:
(8*1)+(7*0)+(6*5)+(5*8)+(4*8)+(3*7)+(2*2)+(1*3)=138
138 % 10 = 8
So 105887-23-8 is a valid CAS Registry Number.

105887-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-oxo-1,2-diphenylethyl) 3-phenylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,3-phenyl-,2-oxo-1,2-diphenylethyl ester

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:105887-23-8 SDS

105887-23-8Relevant articles and documents

Synthesis of functionalized γ-lactones via a three-component cascade reaction catalyzed by consecutive N-heterocyclic carbene systems

Zhao, Qian,Han, Bo,Wang, Biao,Leng, Hai-Jun,Peng, Cheng,Huang, Wei

, p. 26972 - 26976 (2015)

Two consecutive N-heterocyclic carbene (NHC) catalytic systems were combined in a one-pot cascade reaction for the assembly of aromatic aldehydes and 2-haloenals into a structurally complex γ-lactone backbone. To our knowledge, this is the first report of NHC-catalyzed [3 + 2] annulation of α,β-unsaturated acylazoliums with 1,2-bisnucleophiles.

Lipophilic NHC assisted one-pot synthesis of syncarpamide analogues in aqueous medium

Suresh, Pavithira,Selva Ganesan, Subramaniapillai

, p. 6257 - 6261 (2019/04/25)

Lipophilic NHC catalysis in aqueous medium was reported for the synthesis of biologically relevant (a)symmetrically substituted and unsymmetrically substituted syncarpamide analogues. All the reported reactions were performed in the absence of any expensive metal salts or additives. A diverse array of syncarpamide analogues was obtained in good yields. Lipophilic NHC catalysis was also extended to chemoselective transesterification reactions.

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