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2-Amino-3-(3,5-dihydroxyphenyl)propanoic acid, also known as L-DOPA, is a naturally occurring amino acid that serves as a precursor to neurotransmitters such as dopamine, norepinephrine, and epinephrine. It is characterized by a central amino group attached to a carbon chain with a hydroxyl group and a dihydroxyphenyl ring, which imparts its significant biological properties.

587-62-2

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587-62-2 Usage

Uses

Used in Pharmaceutical Industry:
L-DOPA is utilized as a medication for the treatment of Parkinson's disease and other conditions related to dopamine deficiency. It helps alleviate symptoms by increasing the levels of dopamine in the brain.
Used in Neurological Disorder Treatment:
L-DOPA has been studied for its potential use in treating depression, schizophrenia, and other neurological disorders, due to its role in neurotransmission and its influence on brain chemistry.
Used in Cosmetics Industry:
As an important compound in the biosynthesis of melanin, L-DOPA is also used in the cosmetics industry for its effects on skin and hair pigmentation, contributing to the development of products that address color-related cosmetic concerns.

Check Digit Verification of cas no

The CAS Registry Mumber 587-62-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 587-62:
(5*5)+(4*8)+(3*7)+(2*6)+(1*2)=92
92 % 10 = 2
So 587-62-2 is a valid CAS Registry Number.

587-62-2SDS

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 2-amino-3-(3,5-dihydroxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 3,5-dihydroxy-phenylalanine

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:587-62-2 SDS

587-62-2Downstream Products

587-62-2Relevant academic research and scientific papers

NOVEL MULTIMERIC MOLECULES, A PROCESS FOR PREPARING THE SAME AND THE USE THEREOF FOR MANUFACTURING MEDICINAL DRUGS

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, (2010/06/16)

The invention relates to a compound of the formula (I): in which k and j are independently 0 or 1, Y is a macrocycle in which the cycle includes 9 to 36 carbon atoms and is functionalised by three amino functions and by a chain for attaching the spacer arm Z via an X bond, Rc is a binding pattern with a receptor of the TNF superfamily, X is a chemical function for binding the Y group to the space arm, and Z is a bi-, tri- or tetra-functional spacer arm.

NOVEL MULTIMERIC CD40 LIGANDS, METHOD FOR PREPARING SAME AND USE THEREOF FOR PREPARING DRUGS

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, (2010/08/07)

The invention concerns a compound of formula (I), wherein Y represents a macrocycle whereof the cycle comprises 9 to 36 atoms, and is functionalized by three amine or COOH functions; Rc represents a group of formula H—Xa—Xb—Xc—Xd—Xe—(Xf)i—, wherein i represents 0 or 1, Xn is in particular selected among lysine, arginine, ornithine residues, Xb is in particular selected among glycine, asparagine, L-proline or D-proline residues, Xc et Xd are in particular selected among tyrosine, phenylalanine or 3-nitrotyrosine residues, Xe et Xf are in particular selected among the following amino acid residues: NH2—(CH2)n—COOH, n ranging from 1 to 10 or NH2—(CH2—CH2—O)m—CH2CH2COOH, m ranging from 3 to 6, provided that one at least of the amino acid residues Xa, Xb, Xc and Xd is different from the corresponding amino acid in the sequence of the natural CD40 143Lys-Gly-Tyr-Tyr146 fragment

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