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Fmoc-7-hydroxy-(r)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is a specialized chemical compound derived from the amino acid tetrahydroisoquinoline. It features a 7-hydroxy group, a carboxylic acid functional group, and a fluorenylmethyloxycarbonyl (Fmoc) protecting group. Fmoc-7-hydroxy-(r)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid plays a significant role in the field of organic chemistry, particularly in the synthesis of peptides and proteins, as well as in medicinal chemistry research. Its distinctive structure and reactivity contribute to the development of a wide range of molecular structures and potential pharmaceutical agents.

178432-50-3

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178432-50-3 Usage

Uses

Used in Organic Chemistry:
Fmoc-7-hydroxy-(r)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is used as a building block in the synthesis of complex organic molecules. Its unique functional groups facilitate the formation of various molecular structures, making it a valuable component in organic chemistry.
Used in Peptide and Protein Synthesis:
In the field of peptide and protein synthesis, Fmoc-7-hydroxy-(r)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid serves as a key component. Its incorporation into peptide chains allows for the creation of proteins with specific functions and properties, contributing to advancements in biotechnology and pharmaceuticals.
Used in Medicinal Chemistry Research:
Fmoc-7-hydroxy-(r)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is utilized as a research tool in medicinal chemistry. Its reactivity and structural features make it suitable for the development of new pharmaceutical agents, potentially leading to the discovery of novel treatments and therapies.
Used in Drug Development:
In the pharmaceutical industry, Fmoc-7-hydroxy-(r)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is used as a precursor in the development of new drugs. Its unique properties enable the design and synthesis of innovative molecular entities with potential therapeutic applications.
Used in Chemical Synthesis Education:
Fmoc-7-hydroxy-(r)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid also serves as an educational tool in teaching chemical synthesis techniques. Its versatile reactivity allows students and researchers to explore various synthetic pathways and develop a deeper understanding of organic chemistry principles.

Check Digit Verification of cas no

The CAS Registry Mumber 178432-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,4,3 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 178432-50:
(8*1)+(7*7)+(6*8)+(5*4)+(4*3)+(3*2)+(2*5)+(1*0)=153
153 % 10 = 3
So 178432-50-3 is a valid CAS Registry Number.

178432-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-hydroxy-D-Tic-OH

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:178432-50-3 SDS

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