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N-T-BOC-B-ALA-TRP-MET-ASP(BENZYL)-PHEAMI DE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88463-49-4

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88463-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88463-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,6 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88463-49:
(7*8)+(6*8)+(5*4)+(4*6)+(3*3)+(2*4)+(1*9)=174
174 % 10 = 4
So 88463-49-4 is a valid CAS Registry Number.

88463-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Phenylalaninamide, N-[(1,1-dimethylethoxy)carbonyl]-β-alanyl-L-tryptophyl-L-methionyl-L-α-aspartyl-, phenylmethyl ester

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:88463-49-4 SDS

88463-49-4Downstream Products

88463-49-4Relevant academic research and scientific papers

Microwave-assisted solution phase peptide synthesis in neat water

Mahindra, Amit,Nooney, Karthik,Uraon, Shrikant,Sharma, Krishna K.,Jain, Rahul

, p. 16810 - 16816 (2013/09/23)

An environmentally benign protocol for solution phase peptide synthesis has been developed in neat water using TBTU/HOBt/DIEA as a coupling combination under microwave irradiation. Key features of this procedure are the replacement of commonly used toxic organic solvents like DMF and NMP, the use of lower amounts of reactants, compatibility with both N-α-Boc- and N-α-Fmoc-protected amino acids and all commonly used side-chain protective groups, short reaction time, and racemization-free synthesis in high yield and purity. The Royal Society of Chemistry 2013.

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