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64578-11-6

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64578-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64578-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,7 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64578-11:
(7*6)+(6*4)+(5*5)+(4*7)+(3*8)+(2*1)+(1*1)=146
146 % 10 = 6
So 64578-11-6 is a valid CAS Registry Number.

64578-11-6SDS

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 N-(benzyloxycarbonyl)-L-aspartic acid-4-chloride-1-benzyl ester

1.2 Other means of identification

Product number -
Other names N-Benzyloxycarbonyl-L-asparaginsaeure-1-benzylester-4-chlorid

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:64578-11-6 SDS

64578-11-6Upstream product

64578-11-6Relevant articles and documents

Towards a biomimetic synthesis of barrenazine A

Buron, Frédéric,Turck, Alain,Plé, Nelly,Bischoff, Laurent,Marsais, Francis

, p. 4327 - 4330 (2008/02/04)

We report herein a concise and biomimetic synthesis of a precursor of barrenazine A, a cytotoxic alkaloid. The C2-symmetry of this molecule suggested the dimerization of an aminoketone, as the precursor of the central core pyrazine. This compou

Synthesis of suitably protected hydroxymethylene phosphonate- and 'phosphate phosphonate'-analogues of phosphoserine and their incorporation into synthetic peptides

Wiemann, Arndt,Frank, Ronald,Tegge, Werner

, p. 1331 - 1337 (2007/10/03)

Two suitably protected derivatives of phosphoserine 1 have been prepared in which the regular ester-oxygen is replaced by either a hydroxymethylene moiety or by a phosphorylated hydroxymethylene moiety. The second derivative termed 'phosphate phosphonate'

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