18952-34-6

Basic information

• Product Name: (1S,3S)-cycloheptane-1,3-diol
• Synonyms: 1,3-cycloheptanediol, (1S,3S)-
• CAS NO: 18952-34-6
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.18
• Mol File: 18952-34-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 263.9°C at 760 mmHg
• Flash Point: 128.4°C
• Density: 1.101g/cm³
• Vapor Pressure: 0.0014mmHg at 25°C
• Refractive Index: 1.512
• CAS DataBase Reference: (1S,3S)-cycloheptane-1,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3S)-cycloheptane-1,3-diol(18952-34-6)
• EPA Substance Registry System: (1S,3S)-cycloheptane-1,3-diol(18952-34-6)

Safety Data

• Hazardous Substances Data: 18952-34-6(Hazardous Substances Data)

Upstream product

• 74676-71-4 1α,3β-bis(methoxymethoxy)-cycloheptane 
• 74676-69-0 2β-bromo-1α,3β-dihydroxycycloheptane 
• 74676-70-3 2β-bromo-1α,3β-bis(methoxymethoxy)-cycloheptane 
• 36291-49-3 3-bromocycloheptene 
• 79605-67-7 2-cycloheptenol 
• 1194-18-9 cycloheptane-1,3-dione 
• 89858-82-2 endo-8-oxabicyclo[3.2.1]oct-6-en-3-ol 
• 18952-34-6 (±)-1,3-cycloheptanediol 

Downstream Products

• 1121-66-0 2-Cyclohepten-1-one 
• 1431136-90-1 (S)-3-hydroxycycloheptanone 
• 18952-34-6 (R,R)-1,3-cycloheptanediol 

Relevant articles and documents

SYNTHESIS AND APPLICATION OF CHIRAL SUBSTITUTED POLYVINYLPYRROLIDINONES

Chiral polyvinylpyrrolidinone (CSPVP), complexes of CSPVP with a core species, such as a metallic nanocluster catalyst, and enantioselective oxidation reactions utilizing such complexes are disclosed. The CSPVP complexes can be used in asymmetric oxidation of diols, enantioselective oxidation of alkenes, and carbon-carbon bond forming reactions, for example. The CSPVP can also be complexed with biomolecules such as proteins, DNA, and RNA, and used as nanocarriers for siRNA or dsRNA delivery.

Efficient ruthenium-catalyzed transfer hydrogenation/hydrogenation of 1,3-cycloalkanediones to 1,3-cycloalkanediols using microwave heating

A number of 1,3-cycloalkanediones were efficiently reduced to the corresponding diols in good yield by the use of a ruthenium catalyst, 2-propanol, and hydrogen gas under microwave heating.

Reduktive Ringoeffnung von Oxabicyclen mit Diisobutylaluminiumhydrid - Anwendung bei der Synthese der C17-C23-Untereinheit von Ionomycin

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