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(S)-3,4-Dihydroxybutyramide, with the molecular formula C4H9NO3, is an amide derivative of 3,4-dihydroxybutyric acid, a metabolite of dopamine. This chemical compound has garnered interest for its potential therapeutic applications in conditions related to dopamine dysregulation, such as Parkinson's disease and schizophrenia. It also shows promise as a chiral building block in synthetic chemistry for the creation of biologically active compounds and as a potential biomarker for neurological disorders due to its association with dopamine metabolism in the brain.

126495-84-9

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126495-84-9 Usage

Uses

Used in Pharmaceutical Industry:
(S)-3,4-Dihydroxybutyramide is used as a potential therapeutic agent for neurological conditions characterized by dopamine dysregulation, such as Parkinson's disease and schizophrenia. Its role in modulating dopamine levels makes it a candidate for treating these conditions.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, (S)-3,4-Dihydroxybutyramide serves as a chiral building block, facilitating the synthesis of other biologically active compounds. Its unique structure contributes to the development of new pharmaceuticals and chemical entities.
Used in Diagnostics:
(S)-3,4-Dihydroxybutyramide is investigated as a potential biomarker for certain neurological disorders. Its correlation with dopamine metabolism in the brain suggests its utility in diagnosing and monitoring the progression of these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 126495-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,9 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126495-84:
(8*1)+(7*2)+(6*6)+(5*4)+(4*9)+(3*5)+(2*8)+(1*4)=149
149 % 10 = 9
So 126495-84-9 is a valid CAS Registry Number.

126495-84-9SDS

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 3,4-dihydroxybutanamide

1.2 Other means of identification

Product number -
Other names 3.4-dihydroxybutyramide

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:126495-84-9 SDS

126495-84-9Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF PROTECTED DIHYDROXYPROPYL TRIALKYLAMMONIUM SALTS AND DERIVATIVES THEREOF

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Page/Page column 5; 7; 8-9, (2008/06/13)

A process for the preparation of protected dihydroxypropyl trialkylammonium salts, particularly in chiral form is described. In particular, a process for the preparation of (2,2-dimethyl-1,3-dioxolan-4-ylmethyl)trialkylammonium salts, particularly in chiral form is described. Furthermore, a process is described wherein the (2,2-dimethyl-1,3-dioxolan-4ylmethyl)trialkylammonium salts is a 2,2-dimethyl-1,3-dioxolan-4-ylmethyl trimethylammonium salt, preferably in chiral form. The protected dihydroxypropyl trialkylammonium salts lead to L-carnitine (9) when in chiral form (5).

New synthesis of chiral 1,3-oxazinan-2-ones from carbohydrate derivatives

Ella-Menye, Jean-Rene,Sharma, Vibha,Wang, Guijun

, p. 463 - 469 (2007/10/03)

(Chemical Equation Presented) Chiral 1,3-oxazinan-2-ones are useful intermediates in synthesizing pharmaceutical compounds and amino alcohols. In this paper, we report a new synthetic method to chiral 6-hydroxymethyl 1,3-oxazinan-2-ones and their analogue

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