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Sulfuric acid, diphenyl ester, also known as diphenyl sulfate or phenyl hydrogen sulfate, is an organic compound with the chemical formula C12H10O4S. It is a colorless, crystalline solid that is soluble in organic solvents and slightly soluble in water. Sulfuric acid, diphenyl ester is formed by the reaction of sulfuric acid with two molecules of phenol, resulting in the esterification of the acid. Diphenyl sulfate is used as an intermediate in the synthesis of various organic compounds, such as pharmaceuticals, dyes, and other chemicals. It is also employed as a reagent in organic synthesis and as a catalyst in certain reactions. Due to its reactivity and potential hazards, it is important to handle diphenyl sulfate with care, following proper safety protocols.

4074-56-0

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4074-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4074-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4074-56:
(6*4)+(5*0)+(4*7)+(3*4)+(2*5)+(1*6)=80
80 % 10 = 0
So 4074-56-0 is a valid CAS Registry Number.

4074-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenyl sulfate

1.2 Other means of identification

Product number -
Other names Schwefelsaeure-diphenylester

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:4074-56-0 SDS

4074-56-0Relevant academic research and scientific papers

SuFEx-based synthesis of polysulfates

Dong, Jiajia,Sharpless, K. Barry,Kwisnek, Luke,Oakdale, James S.,Fokin, Valery V.

supporting information, p. 9466 - 9470 (2014/11/07)

High-molecular-weight polysulfates are readily formed from aromatic bis(silyl ethers) and bis(fluorosulfates) in the presence of a base catalyst. The reaction is fast and proceeds well under neat conditions or in solvents, such as dimethyl formamide or N-methylpyrrolidone, to provide the desired polymers in nearly quantitative yield. These polymers are more resistant to chemical degradation than their polycarbonate analogues and exhibit excellent mechanical, optical, and oxygen-barrier properties. High-molecular-weight polysulfates are readily formed from aromatic bis(silyl ethers) and bis(fluorosulfates) in the presence of a base catalyst. The polymers were obtained in nearly quantitative yield under neat conditions, they are more resistant to chemical degradation than their polycarbonate analogues and exhibit excellent mechanical, optical, and oxygen-barrier properties. BPA=bisphenol A.

Biaryl construction through kumada coupling with diaryl sulfates as one-by-one electrophiles under mild conditions

Guan, Bing-Tao,Lu, Xing-Yu,Zheng, Yang,Yu, Da-Gang,Wu, Tong,Li, Kun-N,Li, Bi-Jie,Shi, Zhang-Jie

supporting information; experimental part, p. 396 - 399 (2010/03/04)

(Figure presented) Diaryl sulfates were successfully applied as one-by-one organo electrophiles in Kumada coupling to construct biaryls with the emission of harmless Inorganic salts.

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