114362-79-7

Basic information

• Product Name: 3-Thiophenemethanol, 2,3-dihydro-a-phenyl-, 1,1-dioxide
• CAS NO: 114362-79-7
• Molecular Formula: C11H12O3S
• Molecular Weight: 224.28
• Mol File: 114362-79-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Thiophenemethanol, 2,3-dihydro-a-phenyl-, 1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Thiophenemethanol, 2,3-dihydro-a-phenyl-, 1,1-dioxide(114362-79-7)
• EPA Substance Registry System: 3-Thiophenemethanol, 2,3-dihydro-a-phenyl-, 1,1-dioxide(114362-79-7)

Safety Data

• Hazardous Substances Data: 114362-79-7(Hazardous Substances Data)

Upstream product

• 53336-42-8 3-bromo-2,3-dihydro-thiophene-1,1-dioxide 
• 100-52-7 benzaldehyde 
• 77-79-2 3-Sulfolene 

Downstream Products

• 122236-30-0 3-<(phenylthio)benzyl>-3-sulfolene 
• 122236-34-4 3-(phenylthio)-4-benzyl-3-sulfolene 

Relevant articles and documents

The Effect of Lithium Ion on the Regioselectivity of Substitution Reactions of Zinc Sulfolenylate

The addition of lithium cation to zinc sulfolenylates significantly changes the regioselectivity of its reaction toward carbonyl electrophiles. The more lithium salt is added, the more the reactions prefer to take place at the α-position of the sulfolenyl

Regioselective Synthesis of 3-Acylated 2,5-Dihydrothiophene S,S-Dioxides via Ultrasound-promoted Allylzincation of 3-Bromo-2,3-dihydrothiophene S,S-Dioxide

3-Acylated 2,5-dihydrothiophene S,S-dioxides were synthesized from 3-hydroxyalkylated 2,3-dihydrothiophene S,S-dioxides, prepared highly regioselectively via ultrasound-promoted allylzincation of 3-bromo-2,3-dihydrothiophene S,S-dioxide.