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596846-89-8

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596846-89-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596846-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,8,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 596846-89:
(8*5)+(7*9)+(6*6)+(5*8)+(4*4)+(3*6)+(2*8)+(1*9)=238
238 % 10 = 8
So 596846-89-8 is a valid CAS Registry Number.

596846-89-8SDS

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 trans-NH-L-(5-allyl)Pro-OMe

1.2 Other means of identification

Product number -
Other names (2S,5S)-5-Allyl-pyrrolidine-2-carboxylic acid methyl 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:596846-89-8 SDS

596846-89-8Downstream Products

596846-89-8Relevant articles and documents

Synthesis of hydrophobic phase-tagged prolyl peptides featuring rapid reaction/separation

Chiba, Kazuhiro,Sugihara, Mari,Yoshida, Kazumi,Mikami, Yuzuru,Kim, Shokaku

experimental part, p. 8014 - 8020 (2009/12/06)

Hydrophobically tagged prolyl peptides were synthesized using an electrochemically modified prolyl moiety. The hydrophobic tag served a useful handle for the repetitive reaction/separation steps during solution-phase peptide synthesis. Furthermore, the ta

Synthesis of new bicyclic lactam peptidomimetics by ring-closing metathesis reactions

Colombo, Lino,Di Giacomo, Marcello,Vinci, Valerio,Colombo, Matteo,Manzoni, Leonardo,Scolastico, Carlo

, p. 4501 - 4513 (2007/10/03)

An efficient and versatile synthetic method for the preparation of new fused bicyclic lactams 3a and 3b is described. The spirane cyclopentane nucleus was easily installed by diallylation of the pyroglutamate derivative 18 followed by ring-closing metathe

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