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Butanoic acid, 2-bromo-, 2,6-dimethoxyphenyl ester is a complex organic compound with the chemical formula C11H15BrO4. It is an ester derivative of butanoic acid, featuring a 2-bromo substituent and a 2,6-dimethoxyphenyl group. Butanoic acid, 2-bromo-, 2,6-dimethoxyphenyl ester is characterized by its molecular structure, which includes a four-carbon butanoic acid chain, a bromine atom attached to the second carbon, and a phenyl ring with two methoxy groups at the 2nd and 6th positions. The ester linkage is formed between the carboxylic acid group of butanoic acid and the hydroxyl group of the 2,6-dimethoxyphenol. This chemical is primarily used in research and development, particularly in the synthesis of pharmaceuticals and other organic compounds, due to its unique structure and reactivity.

1440-82-0

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1440-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1440-82:
(6*1)+(5*4)+(4*4)+(3*0)+(2*8)+(1*2)=60
60 % 10 = 0
So 1440-82-0 is a valid CAS Registry Number.

1440-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,6-dimethoxyphenyl) 2-bromobutanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid,2-bromo-,2,6-dimethoxyphenyl ester

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:1440-82-0 SDS

1440-82-0Relevant academic research and scientific papers

α-amino acid phenolic ester derivatives: Novel water-soluble general anesthetic agents which allosterically modulate gabaa receptors

Anderson,Belelli,Bennett,Buchanan,Casula,Cooke,Feilden,Gemmell,Hamilton,Hutchinson,Lambert,Maidment,McGuire,McPhail,Miller,Muntoni,Peters,Sansbury,Stevenson,Sundaramt

, p. 3582 - 3591 (2007/10/03)

In the search for a novel water-soluble general anesthetic agent the activity of an α-amino acid phenolic ester lead, identified from patent literature, was markedly improved. In addition to improving in vivo activity in mice, good in vitro activity at GABAA receptors was also conferred. Within the series of compounds good enantioselectivity for both in vitro and in vivo activity was found, supporting a protein-mediated mechanism of action for anesthesia involving allosteric modulation of GABAA receptors. α-Amino acid phenolic ester 19, as the hydrobromide salt Org 25435, was selected for clinical evaluation since it retained the best overall anesthetic profile coupled with improved stability and water solubility. In the clinic it proved to be an effective intravenous anesthetic in man with rapid onset of and recovery from anesthesia at doses of 3 and 4 mg/kg.

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