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

54064-02-7

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54064-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54064-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,6 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54064-02:
(7*5)+(6*4)+(5*0)+(4*6)+(3*4)+(2*0)+(1*2)=97
97 % 10 = 7
So 54064-02-7 is a valid CAS Registry Number.

54064-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[(2S)-1-oxo-1-phenylpropan-2-yl]carbamate

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:54064-02-7 SDS

54064-02-7Relevant academic research and scientific papers

A practical one-pot process for α-amino aryl ketone synthesis

Conrad, Karen,Hsiao, Yi,Miller, Ross

, p. 8587 - 8589 (2005)

An efficient, convenient, high-yielding synthesis of α-amino aryl ketones is described, involving the one-pot deprotonation-transmetallation- arylation of a Weinreb amide while retaining chirality of the original amide.

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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