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171820-73-8

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171820-73-8 Usage

General Description

Boc-Dab(Aloc)-OH is a chemical compound that is used in the field of organic chemistry. The "Boc" in the name refers to the tert-butyloxycarbonyl protecting group, which is commonly used to protect amines during chemical reactions. "Dab" stands for 2,2-diaminobutyric acid, which is an amino acid derivative that can be used in peptide synthesis. "Aloc" refers to the allyloxycarbonyl protecting group, which is also used to protect amines. Finally, "OH" indicates that the compound has a hydroxyl group, or an alcohol functionality. Overall, Boc-Dab(Aloc)-OH is a versatile compound that can be used to protect and modify amino acids and peptides in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 171820-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 171820-73:
(8*1)+(7*7)+(6*1)+(5*8)+(4*2)+(3*0)+(2*7)+(1*3)=128
128 % 10 = 8
So 171820-73-8 is a valid CAS Registry Number.

171820-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-(prop-2-enoxycarbonylamino)butanoic acid

1.2 Other means of identification

Product number -
Other names Nalpha-Boc-Ngamma-allyloxycarbonyl-L-2,4-diaminobutyric acid

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:171820-73-8 SDS

171820-73-8Downstream Products

171820-73-8Relevant articles and documents

An Allyl Protection and Improved Purification Strategy Enables the Synthesis of Functionalized Phosphonamidate Peptides

Cramer, Jonathan,Klebe, Gerhard

supporting information, p. 1857 - 1866 (2017/04/06)

For modern biophysical methods such as isothermal titration calorimetry, high purity of the inhibitor of interest is indispensable. Herein, we describe a procedure for the synthesis and purification of functionalized phosphonamidate peptides that is able to generate inhibitors for the metalloprotease thermolysin for use in biophysical experiments. The method utilizes an allyl ester/alloc protection strategy and takes advantage of a fast and effective solid-phase extraction (SPE) purification step. Applying this strategy, we were able to synthesize a series of highly polar inhibitors featuring amino- and hydroxy-functionalized side chains in excellent purity.

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