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278605-15-5

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278605-15-5 Usage

Description

L-Phenylalanine, 4-ethynylis a chemical compound that belongs to the family of phenylalanine derivatives. It is a modified form of L-phenylalanine with an ethynyl functional group attached to the 4th position of the phenyl ring. This modification endows it with unique properties and potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
L-Phenylalanine, 4-ethynylis used as a precursor for the synthesis of various pharmaceuticals due to its unique ethynyl functional group. This allows for the development of new drugs with novel therapeutic properties.
Used in Neurological Disorders Treatment:
L-Phenylalanine, 4-ethynylis used as a potential treatment for neurological disorders. Its unique structure may offer new avenues for the development of therapies targeting specific neurological conditions.
Used in Chemical and Biochemical Research:
L-Phenylalanine, 4-ethynylis used as a building block in chemical and biochemical research. Its unique properties make it a valuable tool for the development of new synthetic pathways and the study of biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 278605-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,8,6,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 278605-15:
(8*2)+(7*7)+(6*8)+(5*6)+(4*0)+(3*5)+(2*1)+(1*5)=165
165 % 10 = 5
So 278605-15-5 is a valid CAS Registry Number.

278605-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-(4-ethynylphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 4-Ethynyl-L-phenylalanine HCl

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:278605-15-5 SDS

278605-15-5Downstream Products

278605-15-5Relevant articles and documents

An efficient method for the construction of functionalized dna bearing amino acid groups through cross-coupling reactions of nucleoside triphosphates followed by primer extension or PCR

Capek, Petr,Cahova, Hana,Pohl, Radek,Hocek, Michal,Gloeckner, Christian,Marx, Andreas

, p. 6196 - 6203 (2008/02/13)

Single-step aqueous cross-coupling reactions of nucleobase-halogenated 2′-deoxynucleosides (8-bromo-2′-deoxyadenosine, 7-iodo-7-deaza- 2′-deoxyadenosine, or 5-iodo-2′-deoxy-uridine) or their 5′-triphosphates with 4-boronophenylalanine or 4-ethynylphenylal

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