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73401-70-4

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73401-70-4 Usage

General Description

L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-, [4-(carboxymethyl)phenyl]methyl ester is a chemical compound that is commonly used in the field of biochemistry and pharmaceuticals. It is a form of the essential amino acid leucine that is modified to improve its stability and bioavailability. The compound is often used in the formulation of drug delivery systems and as a building block for the synthesis of novel pharmaceutical compounds. Its specific chemical structure allows for controlled release and targeted delivery of drugs, making it a valuable component in the development of new drug formulations. Additionally, it has been studied for its potential bioactive properties and may have applications in the treatment of various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 73401-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,0 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73401-70:
(7*7)+(6*3)+(5*4)+(4*0)+(3*1)+(2*7)+(1*0)=104
104 % 10 = 4
So 73401-70-4 is a valid CAS Registry Number.

73401-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Leu-OMPA

1.2 Other means of identification

Product number -
Other names 2-tert-Butoxycarbonylamino-4-methyl-pentanoic acid 4-carboxymethyl-benzyl ester

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:73401-70-4 SDS

73401-70-4Downstream Products

73401-70-4Relevant articles and documents

Improved synthesis of preformed Boc-aminoacid-bridging groups for use in solid phase peptide synthesis

Calmes,Cavelier,Daunis,Elyacoubi,Jacquier

, p. 2003 - 2006 (2007/10/02)

Preformed Boc-aminoacid-bridging groups are synthesized by an improved method, using Tmse temporary protection of the starting 4-(halomethyl)phenylacetic acid or bromoacetic acid.

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