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199850-05-0

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199850-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199850-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,8,5 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 199850-05:
(8*1)+(7*9)+(6*9)+(5*8)+(4*5)+(3*0)+(2*0)+(1*5)=190
190 % 10 = 0
So 199850-05-0 is a valid CAS Registry Number.

199850-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylethyl 3-phenylprop-2-enoate

1.2 Other means of identification

Product number -
Other names phenylethyl cinnamate

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:199850-05-0 SDS

199850-05-0Downstream Products

199850-05-0Relevant articles and documents

Modified Yamaguchi reagent: Convenient and efficient esterification

Okuno, Yoshinori,Isomura, Shigeki,Nishibayashi, Akihiro,Hosoi, Aiko,Fukuyama, Kei,Ohba, Masashi,Takeda, Kazuyoshi

supporting information, p. 2854 - 2860 (2014/10/15)

A convenient and efficient esterification method that used a modified Yamaguchi reagent (2,4,6-trichlorobenzoyl chloride-4-dimethylaminopyridine) and avoided use not only of intractable acid chloride but also of acid anhydrides was proposed. The reaction mechanism was described by Fourier transform infrared spectroscopy and supported by a density functional theory calculation.

Kinetic resolution of secondary alcohols by NHC-catalyzed oxidative esterification

Desarkar, Suman,Biswas, Anup,Song, Chie Hoon,Studer, Armido

experimental part, p. 1974 - 1983 (2011/07/07)

Kinetic resolution of racemic secondary alcohols by oxidative esterification using carbene catalysis is described. Good to moderate selectivity has been achieved. N-Heterocyclic carbenes (NHCs) were systematically varied and several aldehydes were included in this study as acyl donors. As an oxidant, a readily available bisquinone-type system was used. Georg Thieme Verlag Stuttgart - New York.

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