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10557-66-1

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10557-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10557-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,5 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10557-66:
(7*1)+(6*0)+(5*5)+(4*5)+(3*7)+(2*6)+(1*6)=91
91 % 10 = 1
So 10557-66-1 is a valid CAS Registry Number.

10557-66-1SDS

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 dibutylphosphorylbenzene

1.2 Other means of identification

Product number -
Other names dibutylphenylphosphine oxide

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:10557-66-1 SDS

10557-66-1Downstream Products

10557-66-1Relevant articles and documents

A novel carbon leaving group in the reaction of organometallic compounds with phosphine oxides

Cardellicchio, Cosimo,Fracchiolla, Giuseppe,Naso, Francesco,Tortorella, Paolo,Holody, Wieslawa,Michal Pietrusiewicz

, p. 5773 - 5776 (1999)

The reaction of diphenyl(methoxymethyl)phosphine oxide 1 with organometallic reagents was found to lead to substitution of the methoxymethyl group. The P-phenyl substituent showed a lower propensity to undergo a displacement.

Nickel-catalyzed phosphorylation of aryl triflates with P([Formula presented] compounds

Yang, Jia,Xiao, Jing,Chen, Tieqiao,Han, Li-Biao

, p. 120 - 124 (2016)

A nickel-catalyzed phosphorylation of aryl triflates with P([Formula presented] compounds is disclosed. This reaction can proceed smoothly under a mild reaction condition, producing the corresponding aryl phosphorus compounds in good to high yields.

Selective C-P(O) Bond Cleavage of Organophosphine Oxides by Sodium

Zhang, Jian-Qiu,Ikawa, Eiichi,Fujino, Hiroyoshi,Naganawa, Yuki,Nakajima, Yumiko,Han, Li-Biao

, p. 14166 - 14173 (2020/11/13)

Sodium exhibits better efficacy and selectivity than Li and K for converting Ph3P(O) to Ph2P(OM). The destiny of PhNa co-generated is disclosed. A series of alkyl halides R4X and aryl halides ArX all react with Ph2P(ONa) to produce the corresponding phosphine oxides in good to excellent yields.

General Oxidative Aryl C-P Bond Formation through Palladium-Catalyzed Decarbonylative Coupling of Aroylhydrazides with P(O)H Compounds

Dong, Jianyu,Liu, Long,Ji, Xuyu,Shang, Qian,Liu, Lixin,Su, Lebin,Chen, Bing,Kan, Ruifeng,Zhou, Yongbo,Yin, Shuang-Feng,Han, Li-Biao

supporting information, p. 3198 - 3203 (2019/05/10)

Oxidative C-C/P-H cross-coupling is achieved via Pd-catalyzed decarbonylative cross-coupling of aroylhydrazides with P(O)H compounds. The unique cooperative reaction system, especially the Br?nsted acid and bidentate phosphine ligand, allows the selective activation of the inert C-C bond and the suppression of the undesired oxidation and coordination of >P(O)-H compounds, leading to a general oxidative synthesis of aryl phosphorus compounds from easily available substrates.

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