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4-chloro-3,5-dimethylphenyl diethyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91801-58-0

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91801-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91801-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,0 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91801-58:
(7*9)+(6*1)+(5*8)+(4*0)+(3*1)+(2*5)+(1*8)=130
130 % 10 = 0
So 91801-58-0 is a valid CAS Registry Number.

91801-58-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chloro-3,5-dimethylphenyl) diethyl phosphate

1.2 Other means of identification

Product number -
Other names 4-chloro-3,5-dimethylphenyl diethyl phosphate

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:91801-58-0 SDS

91801-58-0Downstream Products

91801-58-0Relevant academic research and scientific papers

LiI/TBHP Mediated Oxidative Cross-Coupling of P(O)–H Compounds with Phenols and Various Nucleophiles: Direct Access to the Synthesis of Organophosphates

Anitha, Thippani,Ashalu, Kashamalla Chinna,Sandeep, Mummadi,Mohd, Aabid,Wencel-Delord, Joanna,Colobert, Francoise,Reddy, Kallu Rajender

, p. 7463 - 7474 (2019/12/03)

An efficient and mild method for the direct phosphorylation of phenols, alcohols, and amines with P(O)–H has been reported by LiI/TBHP mediated oxidative cross-coupling reaction. Moreover, this protocol extended to β-keto esters for the synthesis of enol phosphates using H-phosphonates. Notably, this developed method applied for the synthesis of organopesticides such as paraoxon, cyanophos, and methyl parathion. The key features of this protocol are mild conditions, short reaction time, good functional group tolerance, and broad substrate scope.

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