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101924-70-3

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101924-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101924-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,2 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101924-70:
(8*1)+(7*0)+(6*1)+(5*9)+(4*2)+(3*4)+(2*7)+(1*0)=93
93 % 10 = 3
So 101924-70-3 is a valid CAS Registry Number.

101924-70-3SDS

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 (R)-methyl 2-(1-(tert-butoxycarbonylamino)-2-phenylethyl)thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Boc-(R)-Phe-Thz-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:101924-70-3 SDS

101924-70-3Downstream Products

101924-70-3Relevant articles and documents

One-pot enantiomeric synthesis of thiazole-containing amino acids: Total synthesis of venturamides A and B

Liu, Yi,He, Peng,Zhang, Yang,Zhang, Xiangyu,Liu, Jun,Du, Yuguo

, p. 3897 - 3905 (2018)

An effective one-pot procedure for enantiomerical synthesis of thiazole-containing amino acid (TCAA) has been established via a cascade disulfide cleavage/thiocarbonylation/intramolecular Staudinger reduction/aza-Wittig/oxidation reaction. Starting from the commercially available amino acid building blocks, a number of TCAAs were prepared in good yields and with excellent optical purities. This method bears features of mild reaction conditions, wide substrate adaptability, and good functional group tolerance. The power of this method was also demonstrated through the concise total synthesis of cyclic hexapeptide Venturamides A and B.

Total syntheses and re-assignment of configurations of the cyclopeptides lissoclinamide 4 and lissoclinamide 5 from Lissoclinum patella

Boden, Christopher D.J.,Pattenden, Gerald

, p. 875 - 882 (2007/10/03)

The total synthesis of lissoclinamide 4 and lissoclinamide 5, which are novel oxazoline/thiazole/thiazoline-based cyclopeptides isolated from the ascidian ("sea squirt") Lissoclinum patella, are described. The synthesis of the bis-thiazole based lissoclin

NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. 55. TOTAL SYNTHESES OF PATELLAMIDES B AND C, CYTOTOXIC CYCLIC PEPTIDES FROM A TUNICATE 1. THEIR PROPOSED STRUCTURES SHOULD BE CORRECTED.

Hamada, Yasumasa,Shibata, Makoto,Shioiri, Takayuki

, p. 5155 - 5158 (2007/10/02)

Patellamides B and C, cytotoxic lipophilic cyclic peptides from a marine tunicate, with proposed structures have been synthesized by the use of diphenyl phosphorazidate(DPPA) and diethyl phosphorocyanidate(DEPC).Their physicochemical properties lead to re

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