199393-63-0

Basic information

• Product Name: (2S)-1-(benzyloxy)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-5,6-dihydro-1,4-dithiin-2-yl)propan-2-ol
• Synonyms: (2S)-1-(benzyloxy)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-5,6-dihydro-1,4-dithiin-2-yl)propan-2-ol
• CAS NO: 199393-63-0
• Molecular Weight: 432.605
• Mol File: 199393-63-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S)-1-(benzyloxy)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-5,6-dihydro-1,4-dithiin-2-yl)propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-1-(benzyloxy)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-5,6-dihydro-1,4-dithiin-2-yl)propan-2-ol(199393-63-0)
• EPA Substance Registry System: (2S)-1-(benzyloxy)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-5,6-dihydro-1,4-dithiin-2-yl)propan-2-ol(199393-63-0)

Safety Data

• Hazardous Substances Data: 199393-63-0(Hazardous Substances Data)

Upstream product

• 199393-75-4 methyl 5,6-dihydro-1,4-dithiine-2-carboxylate 
• 199393-68-5 (5,6-dihydro-1,4-dithiin-2-yl)methanol 
• 61784-35-8 methyl 2-methyl-1,3-dithiolane-2-carboxylate 
• 2930-05-4 (S)-benzyl glycidyl ether 
• 199393-60-7 1-[[O-(p-methoxybenzyl)-oxy]methyl]-5,6-dihydro-1,4-dithiin 

Downstream Products

• 790667-34-4 methyl 6-O-benzyl-4-deoxy-α-D-lyxo-hexopyranoside 
• 790667-37-7 (1R,2S,4S,6R)-4-Benzyloxymethyl-2-methoxy-3,7-dioxa-bicyclo[4.1.0]heptane 
• 790667-36-6 (1S,2S,4S,6S)-4-Benzyloxymethyl-2-methoxy-3,7-dioxa-bicyclo[4.1.0]heptane 
• 790667-32-2 (5S,7S)-7-[(benzyloxy)methyl]-5-methoxy-2,3,7,8-tetrahydro-5H-[1,4]dithiino[2,3-c]pyran 
• 790667-33-3 (5R,7S)-7-[(benzyloxy)methyl]-5-methoxy-2,3,7,8-tetrahydro-5H-[1,4]dithiino[2,3-c]pyran 
• 199393-72-1 Acetic acid (S)-1-benzyloxymethyl-2-(3-formyl-5,6-dihydro-[1,4]dithiin-2-yl)-ethyl ester 
• 130857-02-2 (2S,6S)-2-[(benzyloxy)methyl]-6-methoxy-3,6-dihydro-2H-pyran 
• 199393-67-4 Acetic acid (S)-1-benzyloxymethyl-2-[3-(4-methoxy-benzyloxymethyl)-5,6-dihydro-[1,4]dithiin-2-yl]-ethyl ester 

Relevant articles and documents

Synthesis of 4-deoxy-L-(and D-)hexoses from chiral noncarbohydrate building blocks

4-Deoxy-L-hexoses were synthesized starting from our previously reported reagent 1 and (R)-benzyl glycidyl ether, which led in few steps to a substituted dihydropyran 6. The stereocontrolled hydroxylation of the latter afforded the corresponding 4-deoxy-L

A New and Versatile Allylic Alcohol Anion and Acyl β-Anion Equivalent for Three-Carbon Homologations

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