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67198-87-2

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67198-87-2 Usage

General Description

Boc-D-homoserine is a chemical compound that is commonly used in biochemical and pharmaceutical research. It is an amino acid derivative that is often utilized as a building block for the synthesis of various peptides and proteins. The compound is characterized by its Boc (tert-butoxycarbonyl) protecting group, which helps to protect the amino group during chemical reactions. Boc-D-homoserine has been studied for its potential therapeutic applications, particularly in the fields of immunotherapy and cancer treatment. Overall, this compound plays a critical role in the development of new drugs and medical innovations.

Check Digit Verification of cas no

The CAS Registry Mumber 67198-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67198-87:
(7*6)+(6*7)+(5*1)+(4*9)+(3*8)+(2*8)+(1*7)=172
172 % 10 = 2
So 67198-87-2 is a valid CAS Registry Number.

67198-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-D-Homoserine

1.2 Other means of identification

Product number -
Other names (2R)-4-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic 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:67198-87-2 SDS

67198-87-2Upstream product

67198-87-2Relevant articles and documents

Process for 4-(D-3-amino-3-carboxypropoxy)-phenylglyoxylic acid oxime derivatives

-

, (2008/06/13)

Process for 4-(D-3-amino-3-carboxypropoxy)phenylglyoxylic acid oxime as an amino-protected ester comprising alkylating an amino-protected D-methionine silyl ester with an alkyl or benzyl iodide; cyclizing the alkylsulfonium iodide to an amino-protected D-homoserine lactone; hydrolyzing the lactone to an amino-protected D-homoserine in aqueous base; coupling, to form an ether, the amino-protected D-homoserine as an ester with an ester of 4-hydroxyphenylglyoxylic acid; and forming the oxime of the ether or alternatively coupling the D-homoserine ester with a protected-oxime of an esterified 4-hydroxyphenylglyoxylic acid. The product is useful in preparing the antibiotic FR 1923.

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