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Benzenepropanal, 4-bromo-2,5-dimethoxy, also known as 4-bromo-2,5-dimethoxybenzenepropanal, is an organic compound with the chemical formula C9H11BrO3. It is a derivative of benzenepropanal, featuring a bromine atom at the 4-position, and two methoxy groups at the 2 and 5 positions. Benzenepropanal, 4-broMo-2,5-diMethoxy- is characterized by its aldehyde functional group, which is a carbonyl group (C=O) bonded to a hydrogen atom and an alkyl group. The presence of the bromine atom and methoxy groups significantly influences its chemical properties, making it a potentially useful intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and functional groups, it is typically handled with care in a laboratory setting.

1132701-96-2

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1132701-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1132701-96-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,2,7,0 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1132701-96:
(9*1)+(8*1)+(7*3)+(6*2)+(5*7)+(4*0)+(3*1)+(2*9)+(1*6)=112
112 % 10 = 2
So 1132701-96-2 is a valid CAS Registry Number.

1132701-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-Bromo-2,5-dimethoxyphenyl)propanal

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

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More Details:1132701-96-2 SDS

1132701-96-2Relevant academic research and scientific papers

Organocatalytic enantioselective formal synthesis of HRV 3C-protease inhibitor (1R,3S)-thysanone

Sawant, Rajiv T.,Waghmode, Suresh B.

experimental part, p. 1599 - 1602 (2009/05/09)

A short and efficient organocatalytic enantioselective formal synthesis of HRV 3C-protease inhibitor (1R,3S)-thysanone is achieved in a nine-step with 98.7% enantiomeric excess, by employing l-proline-catalyzed asymmetric α-aminooxylation of aldehyde and

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