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2-Butanone, 4-(dibutylphosphinyl)-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88962-96-3

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88962-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88962-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,6 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88962-96:
(7*8)+(6*8)+(5*9)+(4*6)+(3*2)+(2*9)+(1*6)=203
203 % 10 = 3
So 88962-96-3 is a valid CAS Registry Number.

88962-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-dibutylphosphoryl-4-phenylbutan-2-one

1.2 Other means of identification

Product number -
Other names 2-Butanone,4-(dibutylphosphinyl)-4-phenyl

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:88962-96-3 SDS

88962-96-3Downstream Products

88962-96-3Relevant academic research and scientific papers

TfOH-Catalyzed Phosphinylation of 2,3-Allenols into ?-Ketophosphine Oxides

Zhao, Runmin,Huang, Xianhua,Wang, Minning,Hu, Shanshan,Gao, Yuxing,Xu, Pengxiang,Zhao, Yufen

, p. 8185 - 8195 (2020/09/21)

The first facile and efficient acid-catalyzed direct coupling of a wide range of unprotected 2,3-allenols with arylphosphine oxides was developed, offering a general, one-step approach for the synthesis of structurally diverse ?-ketophosphine oxides accompanied by concurrent C-P/Ca?O bond formation with remarkable functional group tolerance and complete atom-economy under metal- A nd additive-free conditions. Mechanistic studies showed that this transformation involved a rearrangement and a phospha-Michael reaction.

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