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Phosphoric acid, (1Z)-2-bromo-1-phenylethenyl diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31428-82-7

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31428-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31428-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,2 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31428-82:
(7*3)+(6*1)+(5*4)+(4*2)+(3*8)+(2*8)+(1*2)=97
97 % 10 = 7
So 31428-82-7 is a valid CAS Registry Number.

31428-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-1-phenylethenyl) diethyl phosphate

1.2 Other means of identification

Product number -
Other names Z-Diaethyl-1-phenyl-2-bromvinyl-phosphat

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:31428-82-7 SDS

31428-82-7Relevant academic research and scientific papers

β-Bromoenol phosphate as a new precursor for the modular regioselective synthesis of substituted furans

Fernandes, Rushil,Mhaske, Krishna,Narayan, Rishikesh

supporting information, (2021/11/24)

Owing to its importance in various realms of chemistry, furan occupies a position of eminence among heterocycles. Despite the availability of many methodologies for the synthesis of variably substituted furans, a modular convenient synthesis of 2,4-disubstituted furans remains challenging. The present work attempts to bridge that gap through a novel annulation-based approach using feedstock chemicals such as methyl ketones and their easily available derivatives, β-bromoenol phosphates. We have demonstrated a hitherto unknown reactivity of β-bromoenol phosphates which is responsible for the observed regioselectivity. The reaction requires only sodium hydride as the base under mild conditions. The scope of the reaction was found to be broad with the possibility of obtaining even tri-substituted furans besides a variety of 2,4-disubstituted furans. The methodology was applied to obtain synthetically challenging 3-acylfuran derivatives as well. The newly developed methodology is characterized by the modularity, regioselectivity as well as its practicality owing to easily available starting materials and fast reaction times.

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