Welcome to LookChem.com Sign In|Join Free
  • or
BZ-ASP-OME is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82933-21-9

Post Buying Request

82933-21-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

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 academic research and scientific papers

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.

The transformation of histidine side chain to non-coded asparagines

Ranganathan, Subramania,Ranganathan, Darshan,Bhattacharyya, Dipti

, p. 5615 - 5618 (2007/10/02)

The transformation of the histidine side chain to that of Nω-carbamoyl asparagine, Nω-formyl asparagine, Nω-benzoyl asparagine, β-cyano alanine and aspartic acid has been described, involving as the primary step, the Ru(VI

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.

The Transformation of Tryptophan to Aspartic Acid in Peptides

Ranganathan, Subramania,Ranganathan, Darshan,Bhattacharyya, Dipti

, p. 1085 - 1086 (2007/10/02)

The tryptophan side chain is transformed by in situ generated ruthenium(VIII), to that of aspartic acid, in good yields; amulti-step degradation sequence is suggested on the basis of the transformations of tetrahydrocarbazole to adipic acid, valine to isobutyric acid, and phenylalanine to phenylacetic acid.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 82933-21-9