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2-Hydroxyphenyl hydrogen sulfate, also known as 2-hydroxyphenyl hydrogen sulfate (ester), is an organic compound with the chemical formula C6H7O4S. It is a derivative of phenol, where one of the hydrogen atoms on the hydroxyl group is replaced by a sulfate group. 2-hydroxyphenyl hydrogen sulfate is a white crystalline solid that is soluble in water and has a molecular weight of 177.18 g/mol. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is often used in the preparation of esters, which are important building blocks in organic chemistry.

4918-96-1

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4918-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4918-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4918-96:
(6*4)+(5*9)+(4*1)+(3*8)+(2*9)+(1*6)=121
121 % 10 = 1
So 4918-96-1 is a valid CAS Registry Number.

4918-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrocatechol sulfate

1.2 Other means of identification

Product number -
Other names benzene-1,2-diol,sulfuric acid

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:4918-96-1 SDS

4918-96-1Upstream product

4918-96-1Relevant academic research and scientific papers

Aryl sulfotransferase from Haliangium ochraceum: A versatile tool for the sulfation of small molecules

Ayuso-Fernandez, Ivan,Galmes, Miquel A.,Bastida, Agatha,Garcia-Junceda, Eduardo

, p. 1059 - 1065 (2014)

Sulfation is an important molecular modification that regulates essential cellular processes and is also implicated in numerous pathological processes. The enzymes responsible for this reaction in living organisms are sulfotransferases. The gene Hoch-5094 from Haliangium ochraceum is annotated as a putative sulfotransferase. The arylsulfotransferase codified by this gene (HocAST) was expressed heterologously in E. coli and showed aryl sulfotransferase activity. Circular dichroism analysis of HocAST showed a main α/β secondary structure that agrees with the overall structure of other cytosolic sulfotransferases. Interestingly, HocAST was able to use both p-nitrophenyl sulfate and 3'-phosphoadenosine-5'-phosphosulfate (PAPS) as sulfuryl donors contrary to that of aryl sulfate sulfotransferase, which cannot use PAPS as a donor. Regarding the specificity towards the acceptor, HocAST has shown quite a wide scope and was able to accept several mono- and dihydroxylated phenols and other phosphorylated compounds as substrates. Sulfation variations: We prove experimentally that the gene Hoch-5094 from Haliangium ochraceum encodes for an aryl sulfotransferase. The codified enzyme, HocAST, may be a very versatile biocatalyst as it is able to use both p- nitrophenyl sulfate (p-NPS) and 3'-phosphoadenosine-5′-phosphosulfate (PAPS) as donors and transfer the sulfuryl group to several phenolic compounds and biologically relevant phosphorylated molecules. GTP(S)=Guanosine-5′- triphosphate(-5′-sulfate), BiPhOH= 4,4'-Biphenol, BiPhOS=4,4'-Biphenol 4-sulfate.

N-Sulfonyl amine-mediated sulfamation of amines

-

, (2008/06/13)

Primary amines are selectively sulfamated by the two-step process of: A. Contacting the amine in liquid phase at low to moderate temperatures with catechol sulfate thereby forming a catechol sulfate addition product, and B. Hydrolyzing the catecho

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