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15215-74-4

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15215-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15215-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,1 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15215-74:
(7*1)+(6*5)+(5*2)+(4*1)+(3*5)+(2*7)+(1*4)=84
84 % 10 = 4
So 15215-74-4 is a valid CAS Registry Number.

15215-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]amino]-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names tert.-Butanol

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:15215-74-4 SDS

15215-74-4Relevant articles and documents

Visible Enantiomer Discrimination via Diphenylalanine-Based Chiral Supramolecular Self-Assembly on Multiple Platforms

Dou, Xiaoqiu,Feng, Chuanliang,Liu, Jinying,Qin, Minggao,Xing, Chao,Zhang, Yaqian,Zhao, Changli

, p. 2524 - 2533 (2020)

The development of enantioselective recognition is of great significance in medical science and pharmaceutical industry, which associates with the molecular recognition phenomenon widely observed in biological systems. In particular, the facile and straig

Effect of Stereochemistry on Chirality and Gelation Properties of Supramolecular Self-Assemblies

Qin, Minggao,Zhang, Yaqian,Xing, Chao,Yang, Li,Zhao, Changli,Dou, Xiaoqiu,Feng, Chuanliang

, p. 3119 - 3129 (2021/01/20)

Although chiral nanostructures have been fabricated at various structural levels, the transfer and amplification of chirality from molecules to supramolecular self-assemblies are still puzzling, especially for heterochiral molecules. Herein, four series o

On the Role of Chirality in Guiding the Self-Assembly of Peptides

Basak, Shibaji,Singh, Ishwar,Ferranco, Annaleizle,Syed, Jebreil,Kraatz, Heinz-Bernhard

supporting information, p. 13288 - 13292 (2017/10/07)

Homochirality in peptides is crucial in sustaining “like–like” intermolecular interactions that allow the formation of assemblies and aggregates and is ultimately responsible for the resulting material properties. With the help of a series of stereoisomer

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