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L-Dopa ethyl ester hydrochloride is a chemical compound derived from L-Dopa, a naturally occurring neurotransmitter and precursor to dopamine. It is known for its ability to cross the blood-brain barrier more efficiently than L-Dopa, making it a valuable compound in the treatment of neurological conditions.
Used in Pharmaceutical Industry:
L-Dopa ethyl ester hydrochloride is used as a therapeutic agent for the treatment of Parkinson's disease. It is utilized for its ability to cross the blood-brain barrier and convert into dopamine once in the brain, thereby increasing dopamine levels to alleviate the symptoms of Parkinson's disease.
Used in Neurological Treatments:
L-Dopa ethyl ester hydrochloride is used as a precursor to dopamine for the treatment of mood disorders and cognitive impairments. Its role in modulating mood, cognition, and movement in the brain makes it a potential candidate for these applications, given the critical role of dopamine in these functions.

23234-41-5

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23234-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23234-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,3 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23234-41:
(7*2)+(6*3)+(5*2)+(4*3)+(3*4)+(2*4)+(1*1)=75
75 % 10 = 5
So 23234-41-5 is a valid CAS Registry Number.

23234-41-5SDS

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 ethyl 2-amino-3-(3,4-dihydroxyphenyl)propanoate hydrochloride

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:23234-41-5 SDS

23234-41-5Relevant academic research and scientific papers

Synthesis of the Chromophore of Pseudobactin, a Fluorescent Siderophore from Pseudomonas

Kolasa, Teodozyj,Miller, Marvin J.

, p. 4246 - 4255 (2007/10/02)

Protected forms of dihydroxyphenylalanine (DOPA) were converted to the corresponding dihydroquinolin-2-ones 13 by nitration and reductive cyclization.Subsequent N-alkylation with α-halo-γ-aminobutyric acid derivatives provided the carbon framework 12 for the chromophore of pseudobactin.Conversion to protected forms of the fluorescent chromophore 5 was accomplished by reaction of 12 with Lawesson's reagent to produce the corresponding thioamide which was cyclized by reaction with mercuric acetate.

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