134756-62-0

Basic information

• Product Name: <1(S)-(1α,4α,5β)>-4-(acetyloxy)-5-<(benzyloxy)methyl>-2-cyclopenten-1-ol
• Synonyms: <1(S)-(1α,4α,5β)>-4-(acetyloxy)-5-<(benzyloxy)methyl>-2-cyclopenten-1-ol
• CAS NO: 134756-62-0
• Molecular Weight: 262.306
• Mol File: 134756-62-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: <1(S)-(1α,4α,5β)>-4-(acetyloxy)-5-<(benzyloxy)methyl>-2-cyclopenten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: <1(S)-(1α,4α,5β)>-4-(acetyloxy)-5-<(benzyloxy)methyl>-2-cyclopenten-1-ol(134756-62-0)
• EPA Substance Registry System: <1(S)-(1α,4α,5β)>-4-(acetyloxy)-5-<(benzyloxy)methyl>-2-cyclopenten-1-ol(134756-62-0)

Safety Data

• Hazardous Substances Data: 134756-62-0(Hazardous Substances Data)

Upstream product

• 100021-11-2 (1α,2β,3α)-2-(benzyloxymethyl)cyclopent-4-ene-1,3-diol 
• 134756-61-9 (1α,2β,3α)-2-<(benzyloxy)methyl>-4-cyclopentene-1,3-diol diacetate 

Downstream Products

• 134875-85-7 <3a(R)-(3aα,6α,6aα)>-6-<(benzyloxy)methyl>-3,3a,6,6a-tetrahydro-2H-cyclopentoxazol-2-one 
• 134875-87-9 <3a(R)-(3aα,6α,6aα)>-6-<(benzyloxy)methyl>-3,6a-dihydro-N,N-dimethyl-6H-cyclopentoxazol-2-amine 
• 134756-65-3 <1(R)-(1α,2β,3α)>-2-<(benzyloxy)methyl>-4-cyclopentene-1,3-diol monocarbamate 
• 134756-63-1 <1(R)-(1α,4α,5β)>-5-<(benzyloxy)methyl>-4-<(tert-butyldimethylsilyl)oxy>-2-cyclopenten-1-ol 
• 134756-64-2 <1(R)-(1α,4α,5β)>-5-<(benzyloxy)methyl>-4-<(tert-butyldimethylsilyl)oxy>-2-cyclopenten-1-ol carbamate 
• 134756-66-4 3,6-di-O-benzyl-(-)-allosamizoline 
• 124583-64-8 (1S,5R)-8-exo-benzyloxymethyl-3-dimethylamino-6-exo,7-endo-dihydroxy-2-oxa-4-azabicyclo<3.3.0>octan-3-ene 
• 183988-92-3 C₇₃H₉₆N₄O₁₇S₂Si₂ 
• 183988-89-8 Acetic acid (3aS,4S,5S,6R,6aR)-6-benzyloxymethyl-2-dimethylamino-4-hydroxy-4,5,6,6a-tetrahydro-3aH-cyclopentaoxazol-5-yl ester 
• 183988-91-2 (3aR,4S,5S,6S,6aR)-6-Benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-2-dimethylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaoxazol-5-ol 
• 183988-90-1 Acetic acid (3aR,4S,5S,6R,6aR)-6-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-2-dimethylamino-4,5,6,6a-tetrahydro-3aH-cyclopentaoxazol-5-yl ester 
• 184179-63-3 (3aS,6R,6aR)-6-Benzyloxymethyl-3,3a,6,6a-tetrahydro-cyclopentaoxazol-2-one 
• 184179-64-4 ((3aS,6R,6aR)-6-Benzyloxymethyl-6,6a-dihydro-3aH-cyclopentaoxazol-2-yl)-dimethyl-amine 
• 184179-61-1 Carbamic acid (1S,4R,5S)-5-benzyloxymethyl-4-hydroxy-cyclopent-2-enyl ester 

Relevant articles and documents

Preparation of a chiral synthon for an HBV inhibitor: Enzymatic asymmetric hydrolysis of (1α,2β,3α)-2-(benzyloxymethyl)cyclopent-4-ene-1, 3-diol diacetate and enzymatic asymmetric acetylation of (1α,2β, 3α)-2-(benzyloxymethyl)cyclopent-4-ene-1,3-diol

Enantioselective asymmetric hydrolysis of (1α,2β,3α)-2- (benzyloxymethyl)-cyclopent-4-ene-1,3-diol diacetate 1 to the corresponding (+)-monoacetate 2 was carried out using lipase PS-30 from Pseudomonas cepacia or pancreatin. A reaction yield of 85 M % wit

Total synthesis of allosamidin: An application of the sulfonamidoglycosylation of glycals

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