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210750-95-1

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210750-95-1 Usage

General Description

BOC-D-GLN(TRT)-OH is a chemical compound commonly used in peptide synthesis. It is an amino acid derivative with a t-butoxycarbonyl (BOC) protecting group on the N-terminal amine and a trityl (TRT) protecting group on the side chain amine of glutamine. BOC-D-GLN(TRT)-OH is often employed as a building block for the construction of customized peptides in laboratory settings. BOC-D-GLN(TRT)-OH is stable and easily handled, making it a useful reagent for the production of peptides for research, pharmaceutical, and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 210750-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,7,5 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 210750-95:
(8*2)+(7*1)+(6*0)+(5*7)+(4*5)+(3*0)+(2*9)+(1*5)=101
101 % 10 = 1
So 210750-95-1 is a valid CAS Registry Number.

210750-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-D-GLN(TRT)-OH

1.2 Other means of identification

Product number -
Other names -

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:210750-95-1 SDS

210750-95-1Relevant articles and documents

Protected amino acids and process for the preparation thereof

-

, (2008/06/13)

Compounds of the formula I, STR1 in which 'R1 is an amino protective group, and n stands for 1 or 2, R1 denotes hydrogen or an amino protective group, R2 denotes hydrogen or a carboxyl protective group and R3 denotes triphenylmethyl, 4-monomethoxy-trityl or 4,4'-dimethoxy-trityl, and reactive carboxylic acid derivatives of such compounds of the formula I in which R2 stands for hydrogen, are described. These compounds can be used as starting materials for the preparation of peptides. They are more suitable for this than are analogous compounds of the formula I in which R3 denotes hydrogen or one of the carbamoyl protective groups hitherto customary.

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