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102767-82-8

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102767-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102767-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,6 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102767-82:
(8*1)+(7*0)+(6*2)+(5*7)+(4*6)+(3*7)+(2*8)+(1*2)=118
118 % 10 = 8
So 102767-82-8 is a valid CAS Registry Number.

102767-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name o-phenyl 4-methylphenyl(4-methylphenyl)phosphinate

1.2 Other means of identification

Product number -
Other names Di-p-tolyl-phosphinic acid phenyl 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:102767-82-8 SDS

102767-82-8Downstream Products

102767-82-8Relevant articles and documents

Base-promoted selective O-phosphorylation of aryl triflates with P(O)-H compounds

Wang, Mingyue,Yang, Jia,Wang, Shuai,Zhong, Hong

, (2020)

Compared to previous transition metal-catalyzed C-phosphorylation reactions for constructing C–P bonds, in the absence of transition metal catalysts and ligands, a direct O-phosphorylation of aryl triflates selectively occurred with P(O)-H compounds in the presence of a base via the construction of O–P bonds. This transformation proceeds under simple and mild conditions, and provides a new method for the preparation of valuable organophosphoryl compounds from readily available P(O)-H compounds and triflates.

DCC-assisted direct esterification of phosphinic and phosphoric acids with O-nucleophiles

Xiong, Biquan,Wang, Gang,Zhou, Congshan,Liu, Yu,Li, Jiandong,Zhang, Pangliang,Tang, Kewen

supporting information, p. 239 - 244 (2017/11/20)

A novel and efficient dicyclohexylcarbodiimide-promoted protocol for the selective and controllable esterification of P(O)OH compounds using O-nucleophiles (alcohols and phenols) as efficient esterification reagents is described. This method features a high efficiency and good functional-group tolerance, meaning a simple way to synthesize a broad spectrum of phosphinic and phosphoric acid esters from basic starting materials with moderate to excellent yields.

Method for preparing organophosphate compound through efficient esterification of P(O)-OH-containing compound and phenol

-

Paragraph 0038, (2017/09/01)

The invention provides a method for preparing an organophosphate compound through efficient esterification of a P(O)-OH-containing compound and phenol. The method realizes efficient and highly selective synthesis of organophosphate derivatives containing

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