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82933-21-9

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82933-21-9 Usage

Chemical Properties

White fluffy powder

Check Digit Verification of cas no

The CAS Registry Mumber 82933-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,3 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82933-21:
(7*8)+(6*2)+(5*9)+(4*3)+(3*3)+(2*2)+(1*1)=139
139 % 10 = 9
So 82933-21-9 is a valid CAS Registry Number.

82933-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name BZ-ASP-OME

1.2 Other means of identification

Product number -
Other names BZ-ASPARTIC ACID-OME

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:82933-21-9 SDS

82933-21-9Relevant articles and documents

Demonstration of Exclusive α-Peptidation at the Micellar Interface

Ranganathan, Darshan,Ranganathan, Subramania,Singh, Girij Pal,Patel, Bhisma Kumar

, p. 525 - 528 (2007/10/02)

Microreactors, dispersed in iso-octane, harboring water pools and crafted from AOT and co-surfactant condensing agent DODCI, exclusively direct α-peptidation, thus reversing the normal preference of glutamic acid and aspartic acid for side chain carboxyl group amidation.

L-METHIONINE OXIDATION: NOVEL AND UNANTICIPATED TRANSFORMATIONS WITH 4-tBUTYL IODOXYBENZENE

Ranganathan, S.,Ranganathan, D.,Singh, S.K.,Bhattacharyya, D.,Shanthy, S.,Singh, G.P.

, p. 5363 - 5366 (2007/10/02)

4-tButyl iodoxybenzene transforms Bz-Met-OMe to products arising from, S oxidation and C-H insertion followed by degradation.Z-Met(sulfoxide)-OMe is very effective in bringing about ester hydrolysis via intramolecular attack.The S oxidation to sulfoxides and then to sulfones can be monitored and controlled, proceeds with chiral retention, affects neither the peptide bond nor the protecting groups and has been further illustrated with,Z-Gly-Met-OMe, Z-Met-OMe and Z-S(benzyl)-Cys-OMe.

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