17793-95-2

Basic information

• Product Name: CIS-1,2-DIHYDROCATECHOL
• Synonyms: CIS-1,2-DIHYDROCATECHOL;CIS-3,5-CYCLOHEXADIENE-1,2-DIOL;3,5-Cyclohexadiene-1,2-diol;cis-3,5-cyclohexadiene-1,2-diol solution;CIS-3 5-CYCLOHEXADIENE-1 2-DIOL SOLUTIO;CIS-3,5-CYCLOHEXADIENE-1,2-DIOL, 20 WT. % SOLUTION IN ETHYL ACETATE;CIS-1,2-DIHYDROCATECHOL, 20;cis-1,2-Dihydrocatechol, 20% soln. in ethyl acetate
• CAS NO: 17793-95-2
• Molecular Formula: C₆H₈O₂
• Molecular Weight: 112.13
• Mol File: 17793-95-2.mol
• Article Data: 7

Chemical Properties

• Melting Point: 60 °C(Solv: hexane (110-54-3))
• Boiling Point: 226.4°Cat760mmHg
• Flash Point: -3 °C
• Appearance: /
• Density: 0.904 g/mL at 25 °C
• Vapor Pressure: 0.0162mmHg at 25°C
• Refractive Index: n20/D 1.403
• Storage Temp.: −20°C
• PKA: 13.12±0.40(Predicted)
• CAS DataBase Reference: CIS-1,2-DIHYDROCATECHOL(CAS DataBase Reference)
• NIST Chemistry Reference: CIS-1,2-DIHYDROCATECHOL(17793-95-2)
• EPA Substance Registry System: CIS-1,2-DIHYDROCATECHOL(17793-95-2)

Safety Data

• Hazard Codes: F,Xi
• Statements: 11-36/37/38-67-66-36
• Safety Statements: 16-26-36-33-29-23
• RIDADR: UN 1173 3/PG 2
• F: 8-10
• Hazardous Substances Data: 17793-95-2(Hazardous Substances Data)

Usage

General Description

CIS-1,2-DIHYDROCATECHOL, also known as cis-pyrocatechol or 1,2-dihydroxybenzene, is a chemical compound with the molecular formula C6H6O2. It is a colorless, crystalline solid with a faint, pleasant odor, and is soluble in water and ethanol. It is commonly used in organic synthesis, as an intermediate in the production of pharmaceuticals, dyes, and other organic compounds. It is also used as a stabilizer in the production of polymers and a precursor for the synthesis of fragrances and flavors. CIS-1,2-DIHYDROCATECHOL is considered to be relatively low in toxicity and is not known to be carcinogenic, teratogenic, or mutagenic. However, it should be handled with care as it can be irritating to the skin, eyes, and respiratory system.

InChI:InChI=1/C6H8O2/c7-5-3-1-2-4-6(5)8/h1-8H/t5-,6+

Upstream product

• 108-05-4 vinyl acetate 
• 86504-11-2 cis-3,5-cyclohexadiene-1,2-diol diacetate 
• 64287-99-6 trans-1,2-Diacetoxy-4,5-dibromcyclohexan 
• 39078-08-5 rac-(3R,4R,5R,6R)-3,4:5,6-diepoxycyclohex-1-ene 
• 64288-00-2 trans-cyclohexa-3,5-diene-1,2-diyl diacetate 
• 1488-25-1 benzene oxide 
• 36635-14-0 (+/-)-3c,4t,5t,6c-tetrachloro-cyclohexane-1r,2t-diol 
• 41992-55-6 α-3,4,5,6-Tetrachlorocyclohex-1-ene 
• 1165952-91-9 cyclohexa-1,3-diene 
• 71-43-2 benzene 
• 56421-33-1 3t,4c,5c,6t-tetrachloro-cyclohexane-1r,2c-diol 

Downstream Products

• 64330-65-0 cis,cis-2,4-hexadienedial 
• 129662-32-4 trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol 
• 86504-06-5 cis-3,5-cyclohexadiene-1,2-diol dibenzoate 
• 118993-49-0 (3aα,6β,7α,7aα)-6-(benzyloxy)-3a,6,7,7a-tetrahydro-7-hydroxybenzo-1,3-dioxol-2-one 
• 118993-50-3 (3aα,6β,7α,7aα)-6,7-bis(benzyloxy)-3a,6,7,7a-tetrahydrobenzo-1,3-dioxol-2-one 
• 2396-76-1 cis-1,2-diacetoxycyclohexane 
• 4381-96-8 (+/-)-tetra-O-acetylconduritol F 
• 86504-11-2 cis-3,5-cyclohexadiene-1,2-diol diacetate 
• 526-87-4 (+/-)-conduritol C 
• 126814-12-8 (3aα,4α,7α,7aα,8R*,9S*)-3a,4,7,7a-tetrahydro-8,9-dihydroxy-2-phenyl-4,7-ethano-1H-isoindole-1,3(2H)-dione 
• 126814-12-8 (3aα,4α,7α,7aα,8S*,9R*)-3a,4,7,7a-tetrahydro-8,9-dihydroxy-2-phenyl-4,7-ethano-1H-isoindole-1,3(2H)-dione 
• 64288-00-2 trans-cyclohexa-3,5-diene-1,2-diyl diacetate 
• 108-95-2 phenol 

Relevant articles and documents

Enantioselective synthesis of (-)- and (+)-conduritol F via enzymatic asymmetrization of cis-cyclohexa-3,5-diene-1,2-diol

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MICROBIAL OXIDATION IN SYNTHESIS: PREPARATION OF 6-DEOXY CYCLITOL ANALOGUES OF MYO-INOSITOL 1,4,5-TRIPHOSPHATE FROM BENZENE

The novel 6-deoxy, 6-deoxy-6-fluoro and 6-deoxy-6-methyl myo-inositol 1,4,5-triphosphate derivatives (4), (5) and (6) were derived from benzene via microbial oxidation to cis -1,2-dihydroxycyclohexa-3,5-diene (2) and conversion through to the key epoxyace