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Phosphoric acid, 4-(1,1-dimethylethyl)phenyl diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13538-40-4

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13538-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13538-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13538-40:
(7*1)+(6*3)+(5*5)+(4*3)+(3*8)+(2*4)+(1*0)=94
94 % 10 = 4
So 13538-40-4 is a valid CAS Registry Number.

13538-40-4SDS

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 Phosphorsaeure-(4-tert-butylphenylester)-diethylester

1.2 Other means of identification

Product number -
Other names 4-tert-butylphenyl 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:13538-40-4 SDS

13538-40-4Relevant academic research and scientific papers

Electrochemical phosphorylation of arenols and anilines leading to organophosphates and phosphoramidates

Xu, Pan,Zhong, Zijian,Zhou, Aihua

supporting information, p. 5342 - 5347 (2021/06/30)

A practical phosphorylation for generating organophosphates and phosphoramidatesviaelectrochemical dehydrogenative cross-coupling of P(O)H compounds with arenols and anilines is disclosed. This method involves using inorganic iodide salts as both redox catalysts and electrolytes in an undivided cell without the addition of oxidants or bases. A preliminary mechanistic study suggests that radicals are not involved in this process. This method is green and eco-friendly and has good functional group tolerance, high yields and broad substrate scope, with the potential for practical synthesis.

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