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2737-00-0

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2737-00-0 Usage

Organophosphorus compound

Yes, derived from butane with two diethoxyphosphoryloxy functional groups attached.

Common uses

Reagent in organic synthesis, precursor in the production of various other compounds, reactive intermediate in the synthesis of pharmaceuticals and agrochemicals.

Physical properties

Highly flammable, requires careful handling and storage.

Potential applications

Materials science, reagent in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 2737-00-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2737-00:
(6*2)+(5*7)+(4*3)+(3*7)+(2*0)+(1*0)=80
80 % 10 = 0
So 2737-00-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H19O4P/c1-4-7-8-12-13(9,10-5-2)11-6-3/h4-8H2,1-3H3

2737-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl diethyl phosphate

1.2 Other means of identification

Product number -
Other names phosphoric acid butyl ester diethyl 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:2737-00-0 SDS

2737-00-0Relevant articles and documents

Diselenide-Mediated Catalytic Functionalization of Hydrophosphoryl Compounds

Handoko,Benslimane, Zacharia,Arora, Paramjit S.

supporting information, p. 5811 - 5816 (2020/07/27)

We report a diaryldiselenide catalyst for cross-dehydrogenative nucleophilic functionalization of hydrophosphoryl compounds. The proposed organocatalytic cycle closely resembles the mechanism of the Atherton-Todd reaction, with the catalyst serving as a recyclable analogue of the halogenating agent employed in the named reaction. Phosphorus and selenium NMR studies reveal the existence of a P-Se bond intermediate, and structural analyses indicate a stereospecific reaction.

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