121239-62-1

Basic information

• Product Name: (-)-9-pseudo-β-L-idopyranosyladenine
• CAS NO: 121239-62-1
• Molecular Weight: 295.298
• Mol File: 121239-62-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (-)-9-pseudo-β-L-idopyranosyladenine(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-9-pseudo-β-L-idopyranosyladenine(121239-62-1)
• EPA Substance Registry System: (-)-9-pseudo-β-L-idopyranosyladenine(121239-62-1)

Safety Data

• Hazardous Substances Data: 121239-62-1(Hazardous Substances Data)

Upstream product

• 4005-49-6 N-benzoyladenine 
• 121239-66-5 Acetic acid (1S,2S,3R,4S,5R,6S)-3-acetoxy-4-acetoxymethyl-6-(6-benzoylamino-purin-9-yl)-2-benzyloxy-5-nitro-cyclohexyl ester 
• 121239-67-6 Acetic acid (1S,2S,3R,4S,6S)-3-acetoxy-4-acetoxymethyl-6-(6-benzoylamino-purin-9-yl)-2-benzyloxy-cyclohexyl ester 
• 121239-65-4 Acetic acid (1R,2S,5S,6R)-5-acetoxy-2-acetoxymethyl-6-benzyloxy-3-nitro-cyclohex-3-enyl ester 
• 121239-64-3 (1R,2S,3S,4S,6S)-4-(6-Amino-purin-9-yl)-2-benzyloxy-6-hydroxymethyl-cyclohexane-1,3-diol 
• 119951-73-4 Benzoic acid (1R,2R,3S,4S,5R,6S)-2,4-diacetoxy-5-acetylamino-3-benzyloxy-6-nitro-cyclohexylmethyl ester 
• 119951-72-3 Benzoic acid (1R,4S,5R,6R)-4,6-diacetoxy-5-benzyloxy-2-nitro-cyclohex-2-enylmethyl ester 
• 119951-74-5 Benzoic acid (1R,2R,3S,4S,5R)-2,4-diacetoxy-5-acetylamino-3-benzyloxy-cyclohexylmethyl ester 
• 121239-59-6 Benzoic acid (1R,2R,3S,4S,5R,6S)-2,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-3-benzyloxy-6-nitro-cyclohexylmethyl ester 
• 121239-61-0 Benzoic acid (1R,2R,3S,4S,5R)-2,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-3-benzyloxy-cyclohexylmethyl ester 
• 121239-63-2 (1R,2S,3S,4R,6R)-4-(5-Amino-6-chloro-pyrimidin-4-ylamino)-2-benzyloxy-6-hydroxymethyl-cyclohexane-1,3-diol 
• 121239-64-3 (1R,2S,3S,4R,6R)-4-(6-Amino-purin-9-yl)-2-benzyloxy-6-hydroxymethyl-cyclohexane-1,3-diol 

Relevant articles and documents

A new approach to the synthesis of optically active cyclohexane analogs of nucleoside using a Michael-type addition reaction to nitro-cyclohexenes as a key reaction

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