35756-26-4

Basic information

• Product Name: 1,4-Dithiin, 2,3-dihydro-5-phenyl-
• CAS NO: 35756-26-4
• Molecular Formula: C10H10S2
• Molecular Weight: 194.321
• Mol File: 35756-26-4.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 1,4-Dithiin, 2,3-dihydro-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Dithiin, 2,3-dihydro-5-phenyl-(35756-26-4)
• EPA Substance Registry System: 1,4-Dithiin, 2,3-dihydro-5-phenyl-(35756-26-4)

Safety Data

• Hazardous Substances Data: 35756-26-4(Hazardous Substances Data)

Upstream product

• 5769-02-8 2-methyl-2-phenyl[1,3]dithiolane 
• 69382-62-3 ethandithiol 
• 70-11-1 α-bromoacetophenone 
• 540-63-6 ethane-1,2-dithiol 
• 532-27-4 1-chloroacetophenone 
• 5684-32-2 2-methyl-2-phenyl-[1,3]oxathiolane 
• 89614-16-4 trans-2-methyl-2-phenyl-1,3-dithiolane S-oxide 
• 89614-17-5 (Z)-2-methyl-2-phenyl-1,3-dithiolane S-oxide 
• 98-86-2 acetophenone 

Downstream Products

• 35756-13-9 2-phenyl-3-methyl-5,6-dihydro-1,4-dithiin 
• 668441-11-0 2-phenyl-3-[(1'S,2'R)-1'-(2',3'-O-isopropylidene-1',2',3'-trihydroxypropyl)]-5,6-dihydro-1,4-dithiin 
• 157381-04-9 (Z)-1-phenyl-3-hydroxy-heptene 
• 267665-93-0 cis-(1S,5'R)-1-(2',2'-dimethyl-[1',3']dioxolan-4'-yl)-3-phenyl-prop-2-en-ol 
• 267665-94-1 cis-(1R,5'R)-1-(2',2'-dimethyl-[1',3']dioxolan-4'-yl)-3-phenyl-prop-2-en-ol 
• 167777-84-6 trans-(1R,5'R)-1-(2',2'-dimethyl-[1',3']dioxolan-4'-yl)-3-phenyl-prop-2-en-ol 
• 34407-87-9 P 368 
• 141643-05-2 5-(3-Chloro-propyl)-6-phenyl-2,3-dihydro-[1,4]dithiine 
• 141643-02-9 5-Ethyl-6-phenyl-2,3-dihydro-[1,4]dithiine 
• 141643-06-3 Phenyl-(3-phenyl-5,6-dihydro-[1,4]dithiin-2-yl)-methanone 
• 141643-07-4 2,2-Dimethyl-1-(3-phenyl-5,6-dihydro-[1,4]dithiin-2-yl)-propan-1-one 
• 141643-04-1 5-Isopropyl-6-phenyl-2,3-dihydro-[1,4]dithiine 

Relevant articles and documents

A one-pot synthesis of 1,4-dithiins and 1,4-benzodithiins from ketones using the recyclable reagent 1,1′-(ethane-1,2-diyl)dipyridinium bistribromide (EDPBT)

A novel access to 1,4-dithiins and 1,4-benzodithiins from the corresponding ketones in one-pot using the recyclable reagent, 1,1′-(ethane-1,2-diyl)dipyridinium bistribromide (EDPBT) is described. This method is mild, simple, environmentally benign and is

A first example using o-iodoxybenzoic acid (IBX) in combination with tetraethylammonium bromide (TEAB) for ring expansion of 1,3-dithiolanes and 1,3-dithianes

A novel one-pot procedure for the synthesis of dihydro-1,4-dithiins and dihydro-1,4-dithiepines from the corresponding 1,3-dithiolanes and 1,3-dithianes using o-iodoxybenzoic acid (IBX) in combination with tetraethylammonium bromide (TEAB) is described. T

Reactivity of ethanediyl S,S-acetals; 2. Synthesis of 2,3-dihydro-1,4-dithiins

A new, reliable one-step synthesis of 2,3-dihydro-1,4-dithiins from ethanediyl S,S-acetal derivatives of carbonyl compounds is reported.