141873-73-6

Basic information

• Product Name: (1R,2R)-3-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-1-(2-thiazolyl)-1,2,3-propanetriol
• Synonyms: (1R,2R)-3-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-1-(2-thiazolyl)-1,2,3-propanetriol
• CAS NO: 141873-73-6
• Molecular Weight: 453.678
• Mol File: 141873-73-6.mol

Chemical Properties

• CAS DataBase Reference: (1R,2R)-3-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-1-(2-thiazolyl)-1,2,3-propanetriol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-3-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-1-(2-thiazolyl)-1,2,3-propanetriol(141873-73-6)
• EPA Substance Registry System: (1R,2R)-3-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-1-(2-thiazolyl)-1,2,3-propanetriol(141873-73-6)

Safety Data

• Hazardous Substances Data: 141873-73-6(Hazardous Substances Data)

Upstream product

• 141873-71-4 (1R,2R)-1-(2-thiazolyl)-1,2,3-propanetriol 
• 103795-10-4 (2R,3R)-1,2-O-Isopropylidene-3-(2-thiazolyl)-1,2,3-propanetriol 
• 141873-72-5 (1R,2R)-3-O-(tert-butyldiphenylsilyl)-1-(2-thiazolyl)-1,2,3-propanetriol 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 141873-74-7 (E)-(3S,4R)-5-benzyloxy-3,4-O-isopropylidenedioxy-1-(2-thiazolyl)1-pentene 
• 141873-74-7 (Z)-(3S,4R)-5-benzyloxy-3,4-O-isopropylidenedioxy-1-(2-thiazolyl)1-pentene 
• 118319-69-0 (S)-((4S,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-thiazol-2-yl-methanol 
• 141873-78-1 2-[(E)-2-((4S,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-3-methyl-thiazol-3-ium; iodide 
• 141873-75-8 (3R,4R,5R)-3-benzyl(tert-butoxycarbonyl)amino-6-benzyloxy-4,5-isopropylidenedioxyhexanal 
• 141873-77-0 (1R,2R)-3-O-benzyl-1,2-O-isopropylidene-1-(2-thiazolyl)-1,2,3-propanetriol 
• 71806-86-5 (4R,5S)-4,5-bis((benzyloxy)methyl)-2,2-dimethyl-1,3-dioxolane 
• 81801-08-3 4-O-benzyl-2,3-O-isopropylidene-aldehydo-D-erythrose 
• 81801-09-4 4-O-benzyl-2,3-O-isopropylidene-D-threose 

Relevant articles and documents

4-O-benzyl-2,3-O-isopropylidene-D-erythrose and -D-threose from 2,3-O-isopropylidene-D-glyceraldehyde via thiazole intermediates. Synthesis of 2-deoxykanosamine

The adduct derived from 2,3-O-isopropylidene-D-glyceraldehyde and 2-(trimethylsilyl)thiazole is readily converted into the title D-erythrose (50% overal yield) by selective protection of the hydroxy groups and cleavage of the thiazole ring; the D-threose