171963-37-4

Basic information

• Product Name: 3(S),4(S),5(R)-trihydroxy-1-cyclohexene-1-carboxylic acid
• Synonyms: 3(S),4(S),5(R)-trihydroxy-1-cyclohexene-1-carboxylic acid
• CAS NO: 171963-37-4
• Molecular Weight: 174.153
• Mol File: 171963-37-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 3(S),4(S),5(R)-trihydroxy-1-cyclohexene-1-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3(S),4(S),5(R)-trihydroxy-1-cyclohexene-1-carboxylic acid(171963-37-4)
• EPA Substance Registry System: 3(S),4(S),5(R)-trihydroxy-1-cyclohexene-1-carboxylic acid(171963-37-4)

Safety Data

• Hazardous Substances Data: 171963-37-4(Hazardous Substances Data)

Upstream product

• 138-59-0 shikimic acid 
• 40983-58-2 methyl shikimate 
• 1476028-68-8 (3R,4S,5R)-ethyl 3,4-epoxy-5-hydroxycyclohex-1-ene-1-carboxylate 
• 179738-33-1 Benzoic acid (1S,2S,6R)-2-bromo-6-hydroxy-4-methoxycarbonyl-cyclohex-3-enyl ester 
• 179738-32-0 Benzoic acid (1S,2S,6R)-2-chloro-6-hydroxy-4-methoxycarbonyl-cyclohex-3-enyl ester 
• 179738-34-2 (1R,5R,6S)-5-Benzoyloxy-7-oxa-bicyclo[4.1.0]hept-2-ene-3-carboxylic acid methyl ester 
• 78844-86-7 methyl 3(R),4(R)-epoxy-5(R)-hydroxy-1-cyclohexene-1-carboxylate 
• 175546-00-6 3(R),4(R)-epoxy-5(R)-hydroxy-1-cyclohexene-1-carboxylic acid 
• 171963-38-5 methyl [3S-(3α,4β,5α)]-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate 

Downstream Products

• 171963-38-5 methyl [3S-(3α,4β,5α)]-3,4,5-trihydroxy-1-cyclohexene-1-carboxylate 

Relevant articles and documents

(3S,4S,5R)-3,4,5-trihydroxy-1-cyclohexene-carboxylic acid from Sequoiadendron giganteum

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Enzyme-catalyzed resolution of 3,8-dioxatricyclo[3.2.1.02,4]octane-6-carboxylic esters and the application to the synthesis of 3-epishikimic acid

3,8-Dioxatricyclo[3.2.1.02,4]octane-6-carboxylic acid, whose racemic form is readily available on a large scale, is a versatile starting material for the synthesis of carbasugars and carbocyclic biologically active natural products. In this stu

Benzene-free synthesis of phenol

Heating shikimic acid in near-critical water leads to the formation of phenol. Since shikimic acid can now be obtained by the microbial conversion of glucose, a benzene-freer route to phenol could become an alternative to the industrial Hock oxidation of cumene derived from benzene (see scheme).