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149639-95-2

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149639-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149639-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,6,3 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149639-95:
(8*1)+(7*4)+(6*9)+(5*6)+(4*3)+(3*9)+(2*9)+(1*5)=182
182 % 10 = 2
So 149639-95-2 is a valid CAS Registry Number.

149639-95-2SDS

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 Boc-L-Thr(Bn)-NHCH3

1.2 Other means of identification

Product number -
Other names Boc-L-Thr(OBn)-NHMe

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:149639-95-2 SDS

149639-95-2Relevant articles and documents

Thio acid/azide amidation: An improved route to N-acyl sulfonamides

Barlett, Kristin N.,Kolakowski, Robert V.,Katukojvala, Sreenivas,Williams, Lawrence J.

, p. 823 - 826 (2007/10/03)

A one-pot procedure for the conversion of carboxylic acids to N-acyl sulfonamides, via thio acid/azide amidation, is presented. The method is compatible with acid- and base-sensitive amino acid protection. N-Acyl sulfonamide synthesis on solid support, pe

INHIBITORS OF ANTHRAX LETHAL FACTOR

-

Page/Page column 131, (2008/06/13)

Methods, compounds and compositions for preventing and treating anthrax infections by inhibiting Anthrax Lethal Factor (LF) activity.

Total synthesis of thiangazole

Akaji, Kenichi,Kiso, Yoshiaki

, p. 10685 - 10694 (2007/10/03)

A method for total synthesis of thiangazole (1), a tris-thiazoline- oxazole metabolite, is described. The key intermediate 9, a linear tetrapeptide amide composed of three S-benzyl-2-methylcysteine residues and a O-benzyl-threonine amide, was synthesized in 4 steps using 2-chloro-1,3- dimethyl-imidazolidium hexafluorophosphate(CIP)mediated activation. The successive thiazoline/oxazole rings were constructed by TiCl4mediated cycledehydration followed by acid-catalyzed Robinson-Gabriel reaction without difficulty.

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