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Carbamic acid, [(1S)-2-oxo-1-(phenylmethyl)butyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114744-89-7

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114744-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114744-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,4 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114744-89:
(8*1)+(7*1)+(6*4)+(5*7)+(4*4)+(3*4)+(2*8)+(1*9)=127
127 % 10 = 7
So 114744-89-7 is a valid CAS Registry Number.

114744-89-7SDS

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 ((S)-1-Benzyl-2-oxo-butyl)-carbamic acid benzyl ester

1.2 Other means of identification

Product number -
Other names -

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:114744-89-7 SDS

114744-89-7Relevant academic research and scientific papers

New Odorless Protocols for the Synthesis of Aldehydes and Ketones from Thiol Esters

Miyazaki, Tohru,Han-Ya, Yuki,Tokuyama, Hidetoshi,Fukuyama, Tohru

, p. 477 - 480 (2007/10/03)

Dodecanethiol esters derived from odorless dodecanethiol proved to be suitable substrates for Pd-catalyzed reduction with triethylsilane, coupling with organozinc reagents, and coupling with terminal acetylenes.

A novel ketone synthesis by a palladium-catalyzed reaction of thiol esters and organozinc reagents

Tokuyama, Hidetoshi,Yokoshima, Satoshi,Yamashita, Tohru,Fukuyama, Tohru

, p. 3189 - 3192 (2007/10/03)

A variety of ketones have been prepared by a palladium-catalyzed reaction of ethanethiol esters with organozinc reagents. Various functional groups, including esters, ketones, aromatic halides and aldehydes, tolerate the reaction conditions. The reaction can also be applied to the synthesis of α-amino ketones using the corresponding L-α-amino thiol esters without racemization.

A NEW FACILE DIASTEREOCONVERSION OF 2-AMINO ALCOHOLS INVOLVING A NOVEL CYCLOCARBAMATION

Kano, Shinzo,Yokomatsu, Tsutomu,Iwasawa, Haruo,Shibuya, Shiroshi

, p. 6331 - 6334 (2007/10/02)

A new practical method for diastereoconversion of 2-amino alcohols was performed by treatment on N-Cbz- derivatives with trifluoromethanesulfonic anhydride or thionyl chloride, followed by ring cleavage of the resulting oxazolidin-2-ones

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