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730927-12-5

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730927-12-5 Usage

General Description

L-2,5-Dimethoxyphenylalanine is a chemical compound that consists of a phenylalanine molecule with two methoxy groups attached to the 2 and 5 positions on the benzene ring. It is commonly referred to as L-2,5-Dimethoxyphenylalanine or L-DOPA. This chemical is important in the production of neurotransmitters in the brain, particularly dopamine, and is frequently used as a precursor in the synthesis of pharmaceutical drugs. L-DOPA has been studied for its potential therapeutic applications in various neurological and psychiatric disorders, including Parkinson's disease and depression. It is also known for its psychoactive effects and is used recreationally as a psychedelic drug.

Check Digit Verification of cas no

The CAS Registry Mumber 730927-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,0,9,2 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 730927-12:
(8*7)+(7*3)+(6*0)+(5*9)+(4*2)+(3*7)+(2*1)+(1*2)=155
155 % 10 = 5
So 730927-12-5 is a valid CAS Registry Number.

730927-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-(2,5-dimethoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names L-2,5-Dimethoxyphenylalanine

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:730927-12-5 SDS

730927-12-5Downstream Products

730927-12-5Relevant articles and documents

Synthesis of Quinone-Bearing Peptides. Photoinduced Electron-Transfer of Peptide-Bridged Porphyrin-Quinone Molecules

Tamiaki, Hitoshi,Maruyama, Kazuhiro

, p. 1499 - 1502 (1993)

Synthetic peptide-bridged porphyrin-quinone molecules were easily available by use of a precursor for a chiral α-mino acid bearing moiety on the side chain, L-(2,5-dimethoxyphenyl)alanine.Photoinduced electron transfer from porphyrin to quinone in the mol

The synthesis of some analogs of the hallucinogen 1 (2,5 dimethoxy 4 methyl phenyl) 2 aminopropane (DOM). III. Some derivatives of 3 phenylalanine

Coutts,Malicky

, p. 390 - 394 (2007/10/10)

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