4074-55-9

Basic information

• Product Name: Catechol Sulfate
• Synonyms: 1,3,2-Benzodioxathiole, 2,2-dioxide;Catechol Sulfate
• CAS NO: 4074-55-9
• Molecular Formula: C₆H₄O₄S
• Molecular Weight: 190.17384
• Mol File: 4074-55-9.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Catechol Sulfate(CAS DataBase Reference)
• NIST Chemistry Reference: Catechol Sulfate(4074-55-9)
• EPA Substance Registry System: Catechol Sulfate(4074-55-9)

Safety Data

• Hazardous Substances Data: 4074-55-9(Hazardous Substances Data)

Upstream product

• 34789-97-4 pyrocatechol monosodium salt 
• 20244-21-7 sodium catecholate 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 74282-82-9 Cyclohexyl-sulfamic acid 2-hydroxy-phenyl ester 
• 193894-15-4 [(2S,3S,5R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl]-sulfamic acid 2-hydroxy-phenyl ester 
• 203663-35-8 2-hydroxyphenyl N-(1-benzylpiperidin-4-yl)sulfamate 
• 1372972-16-1 C₁₄H₉F₆NO₄S 
• 478260-94-5 C₁₄H₁₅NO₄S 
• 1316251-33-8 C₁₆H₂₄N₂O₆S 
• 392670-36-9 C₁₃H₁₂ClNO₄S 
• 1133725-45-7 2-hydroxyphenyl-N-β-alanine methyl ester sulfamate 
• 1032441-40-9 2-hydroxyphenyl N-butylsulfamate 
• 1032441-52-3 2-hydroxyphenyl N-(2-phenylethyl)sulfamate 
• 1032441-54-5 2-hydroxyphenyl N-(3-phenylpropyl)sulfamate 
• 1032441-56-7 2-hydroxyphenyl N-(4-phenylbutyl)sulfamate 
• 1032441-49-8 2-hydroxyphenyl N-decylsulfamate 
• 1032441-45-4 2-hydroxyphenyl N-hexylsulfamate 

Relevant articles and documents

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Sulfur(VI) fluoride compounds and methods for the preparation thereof

This application describes a compound represented by Formula (I): (I) wherein: Y is a biologically active organic core group comprising one or more of an aryl group, a heteroaryl aryl group, a nonaromatic hydrocarbyl group, and a nonaromatic heterocyclic group, to which Z is covalently bonded; n is 1, 2, 3, 4 or 5; m is 1 or 2; Z is O, NR, or N; X1 is a covalent bond or —CH2CH2—, X2 is O or NR; and R comprises H or a substituted or unsubstituted group selected from an aryl group, a heteroaryl aryl group, a nonaromatic hydrocarbyl group, and a nonaromatic heterocyclic group. Methods of preparing the compounds, methods of using the compounds, and pharmaceutical compositions comprising the compounds are described as well.

Chemically soft solid electrolyte interphase forming additives for lithium-ion batteries

The solid electrolyte interphase (SEI) layer is a key element of lithium-ion batteries (LIBs) enabling stable operation and significantly affecting the cycling performance including life-length. Here we present the concept of chemically soft SEI-forming a

Chiral sulfamide-catalyzed asymmetric Michael addition of protected 3-hydroxypropanal to β-nitrostyrenes

Organocatalytic asymmetric Michael addition of 3-(OTBS)-propanal to β-nitrostyrenes catalyzed by chiral sulfamides was investigated. Good d.r. (up to 80:20) and excellent enantioselectivities (up to >99% ee) were achieved. Both the N-[(1R,2R)-2-aminocyclo