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FMOC-D-ASP-ODMB is a specialized chemical compound utilized in the field of peptide synthesis and research. It is composed of a fluorenylmethoxycarbonyl (FMOC) protecting group, a D-aspartic acid residue, and an ortho-dimethoxybenzyl (ODMB) protecting group. The FMOC group serves to protect the N-terminus of amino acids during peptide synthesis, ensuring that the amino acid sequence is correctly formed. The ODMB group, on the other hand, is employed to protect the side chain of specific amino acids, preventing unwanted reactions that could disrupt the peptide's structure. D-aspartic acid, an enantiomer of the amino acid aspartic acid, contributes unique conformational and functional properties to the peptide, making FMOC-D-ASP-ODMB a valuable component in the study and synthesis of peptides for various applications.

200335-63-3

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200335-63-3 Usage

Uses

Used in Pharmaceutical Research and Development:
FMOC-D-ASP-ODMB is used as a building block in the synthesis of peptides for pharmaceutical applications. Its unique properties allow for the creation of peptides with specific structures and functions, which can be explored for potential therapeutic effects.
Used in Peptide Synthesis:
FMOC-D-ASP-ODMB is used as a protected amino acid in the synthesis of peptides. The protecting groups ensure that the peptide sequence is correctly assembled without unwanted side reactions, facilitating the production of peptides with desired properties.
Used in Academic Research:
FMOC-D-ASP-ODMB is used as a research tool in academic studies. Its incorporation into peptides allows researchers to investigate the effects of D-aspartic acid on peptide structure, function, and interactions with biological systems.
Used in Biochemistry and Molecular Biology:
FMOC-D-ASP-ODMB is used in the study of peptide-protein interactions, enzymatic activity, and other biochemical processes. Its unique properties can provide insights into the mechanisms of peptide function and the role of D-amino acids in biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 200335-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,3,3 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 200335-63:
(8*2)+(7*0)+(6*0)+(5*3)+(4*3)+(3*5)+(2*6)+(1*3)=73
73 % 10 = 3
So 200335-63-3 is a valid CAS Registry Number.

200335-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-D-aspartic acid 1-(2,4-dimethoxybenzyl) 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:200335-63-3 SDS

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