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FMOC-D-ASP-NH2, also known as N-(9-fluorenylmethoxycarbonyl)-D-aspartic acid amide, is a synthetic compound that plays a significant role in the fields of biochemistry and organic chemistry research. As a derivative of the amino acid aspartic acid, it features a FMOC (9-fluorenylmethoxycarbonyl) protecting group on the N-terminus and an amide group on the C-terminus. FMOC-D-ASP-NH2 is recognized for its utility as a building block in the synthesis of peptides and proteins, facilitating the assembly of peptide chains. Furthermore, FMOC-D-ASP-NH2 finds applications in the study of neurotransmitter receptors, contributing to drug development and pharmaceutical research. In essence, FMOC-D-ASP-NH2 is a versatile chemical tool that supports a broad spectrum of scientific endeavors.

200335-41-7

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200335-41-7 Usage

Uses

Used in Peptide and Protein Synthesis:
FMOC-D-ASP-NH2 is used as a building block for the construction of peptide chains, providing a reliable and efficient method for synthesizing complex protein structures. Its presence aids in the stepwise assembly of amino acids, which is crucial for the development of novel therapeutic peptides and proteins.
Used in Pharmaceutical Research:
In the pharmaceutical industry, FMOC-D-ASP-NH2 is utilized as a key component in the synthesis of potential drug candidates. Its role in peptide synthesis allows for the exploration of new drug structures with specific targeting and therapeutic properties.
Used in Neurotransmitter Receptor Studies:
FMOC-D-ASP-NH2 is employed as a research tool in the investigation of neurotransmitter receptors. Its involvement in the synthesis of peptides that can interact with these receptors helps in understanding their mechanisms of action and in the development of drugs that modulate receptor activity.
Used in Drug Development:
FMOC-D-ASP-NH2 contributes to drug development by enabling the creation of peptide-based drugs. Its role in peptide synthesis is vital for the production of molecules with specific binding affinities and biological activities, which can be optimized for therapeutic use.
Overall, FMOC-D-ASP-NH2 is a multifaceted compound with applications spanning across various scientific and industrial domains, including peptide and protein synthesis, pharmaceutical research, neurotransmitter receptor studies, and drug development. Its versatility and utility make it an indispensable asset in the advancement of scientific knowledge and the creation of innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 200335-41-7 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, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 200335-41:
(8*2)+(7*0)+(6*0)+(5*3)+(4*3)+(3*5)+(2*4)+(1*1)=67
67 % 10 = 7
So 200335-41-7 is a valid CAS Registry Number.

200335-41-7SDS

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 (3R)-4-amino-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-D-iAsn

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:200335-41-7 SDS

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