116556-76-4

Basic information

• Product Name: (4S)-4-Benzyloxy-5-hydroxy-2-penten-1-al
• Synonyms: (4S)-4-Benzyloxy-5-hydroxy-2-penten-1-al
• CAS NO: 116556-76-4
• Molecular Weight: 206.241
• Mol File: 116556-76-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4S)-4-Benzyloxy-5-hydroxy-2-penten-1-al(CAS DataBase Reference)
• NIST Chemistry Reference: (4S)-4-Benzyloxy-5-hydroxy-2-penten-1-al(116556-76-4)
• EPA Substance Registry System: (4S)-4-Benzyloxy-5-hydroxy-2-penten-1-al(116556-76-4)

Safety Data

• Hazardous Substances Data: 116556-76-4(Hazardous Substances Data)

Upstream product

• 115220-82-1 (3R,4R)-3,4-Bis-benzyloxy-3,4-dihydro-2H-pyran 
• 496-61-7 1,5-anhydro-2-deoxy-D-erythro-pent-1-enitol 
• 116661-76-8 1,5-anhydro-3,4-di-O-benzyl-2-deoxy-D-erythro-pent-1-enitol 
• 496-62-8 D-xylal 

Downstream Products

• 116556-78-6 (2S)-2-Benzyloxy-3,5-octadien-1-ol 
• 116556-80-0 ethyl 7-hydroxy-6(S)-benzyloxy-2,4-heptadienoate 
• 116556-80-0 Ethyl (6S)-6-benzyloxy-7-hydroxy-2,4-heptadienoate 
• 116556-82-2 Ethyl (6S)-6-benzyloxy-7-tosyloxy-2,4-heptadienoate 
• 116556-82-2 ethyl 7-tosyloxy-6(S)-benzyloxy-2,4-heptadienoate 
• 116556-84-4 Ethyl (6S)-6-hydroxy-7-tosyloxyheptanoate 

Relevant articles and documents

An efficient synthesis of 2,3-dideoxy-α,β-unsaturated carbohydrate enals by mixed Lewis acid (HfCl4 and ZnI2) catalyzed hydration of glycals

A new, efficient method has been developed for converting acyl-, arylalkyl- and alkyl-protected glycals into corresponding 2,3-dideoxy-α,β-unsaturated carbohydrate enals utilizing the in situ generated push-pull effect resulting from the synergistic combi

Benzyl Esters of D- and L-Arabinals as Chiral Synthons in Organic Synthesis

An acidic opening of the benzyl esters of D and L arabinal (1,5-anhydro-2-deoxy-erythro-pent-1-enitol) catalyzed by mercuric sulfate has been proposed as the key step in the preparation of chiral synthons with selectively substituted hydroxy groups.