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1007840-62-1

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1007840-62-1 Usage

General Description

FMOC-D-HOMOCYS(TRT)-OH is a chemical compound consisting of a FMOC (9-fluorenylmethyloxycarbonyl) protective group, a D-homocysteine amino acid, and a trityl (TRT) protective group. FMOC-D-HOMOCYS(TRT)-OH is often used as a building block in peptide synthesis, where the FMOC group serves to protect the amine group of the amino acid, while the TRT group protects the thiol group of homocysteine. Upon completion of the peptide synthesis, these protective groups can be removed to expose the functional groups for further chemical reactions or use in biological studies. FMOC-D-HOMOCYS(TRT)-OH is a valuable tool in the development of peptides and can be used in diverse applications within the field of biochemistry and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 1007840-62-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,8,4 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1007840-62:
(9*1)+(8*0)+(7*0)+(6*7)+(5*8)+(4*4)+(3*0)+(2*6)+(1*2)=121
121 % 10 = 1
So 1007840-62-1 is a valid CAS Registry Number.

1007840-62-1SDS

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 FMOC-D-HOMOCYS(TRT)-OH

1.2 Other means of identification

Product number -
Other names (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tritylthio)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:1007840-62-1 SDS

1007840-62-1Downstream Products

1007840-62-1Relevant articles and documents

Fluorinated and iodinated templates for syntheses of β-turn peptidomimetics

Jiang, Luyong,Burgess, Kevin

, p. 8743 - 8750 (2007/10/03)

Various 2-fluoro-5-nitrobenzoic acids and the homocysteine derivative 2 have been combined in solid phase syntheses of the peptidomimetic types 3-6. NMR and CD data collected for some of these compounds indicate that a transannular SO to HN hydrogen bond stabilizes β-turn conformations for the sulfones and one of the sulfoxide epimers. An extensive library of compounds was made and studied to test this assertion.

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