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22823-50-3

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22823-50-3 Usage

General Description

BOC-MET-OH DCHA is a chemical compound consisting of BOC (tert-butoxycarbonyl) protecting group, methionine (MET) amino acid, and DCHA (dicyclohexylamine) coupling reagent. The BOC group is commonly used to protect amino groups in organic synthesis, while methionine is one of the 20 standard amino acids that are the building blocks of proteins. DCHA, on the other hand, is a coupling reagent used in peptide synthesis to efficiently form amide bonds between the carboxyl and amino groups of amino acids. BOC-MET-OH DCHA is utilized in peptide synthesis and as a building block for the production of peptides and proteins with specific sequences and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 22823-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,2 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22823-50:
(7*2)+(6*2)+(5*8)+(4*2)+(3*3)+(2*5)+(1*0)=93
93 % 10 = 3
So 22823-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H23N.C10H19NO4S/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-10(2,3)15-9(14)11-7(8(12)13)5-6-16-4/h11-13H,1-10H2;7H,5-6H2,1-4H3,(H,11,14)(H,12,13)/t;7-/m.0/s1

22823-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-MET-OH DCHA

1.2 Other means of identification

Product number -
Other names Boc-Met-DCHA

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:22823-50-3 SDS

22823-50-3Relevant articles and documents

Peptide synthesis in aqueous solution. IV. Preparation and properties of [p-(benzyloxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate, [p-(t-butoxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate and [p-(9-fluorenylmethyl-oxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate as water-soluble N-acylating reagents

Azuse,Tamura,Kinomura,Okai,Kouge,Hamatsu,Koizumi

, p. 3103 - 3108 (2007/10/02)

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