(R)-(-)-1-INDANOL

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Names

[ CAS No. ]:
697-64-3

[ Name ]:
(R)-(-)-1-INDANOL

[Synonym ]:
MFCD00064164
2,3-dihydro-1H-inden-1-ol
(R)-2,3-dihydro-1H-inden-1-ol
(-)-(R)-Indan-1-ol
(R)-1-Hydroxyindan
(R)-(-)-1-Indanol

Chemical & Physical Properties

[ Density]:
1.161g/cm3

[ Boiling Point ]:
255.1ºC at 760 mmHg

[ Melting Point ]:
72-73ºC(lit.)

[ Molecular Formula ]:
C9H10O

[ Molecular Weight ]:
134.17500

[ Flash Point ]:
89.2ºC

[ Exact Mass ]:
134.07300

[ PSA ]:
20.23000

[ LogP ]:
1.66620

[ Index of Refraction ]:
1.609

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22-36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2906299090

Synthetic Route

Precursor & DownStream

Precursor

  • 1-Indanone
  • 2,3-Dihydro-1H-inden-1-ol
  • (1R,3S)-3-(ethyldimethylsilyl)-2,3-dihydro-1H-inden-1-ol
  • 1H-Inden-1-ol,2,3-dihydro-, 1-acetate
  • 1H-Inden-1-ol, 2,3-dihydro-, 1-acetate, (1R)
  • isopropyl butyrate
  • Indene
  • Indane

DownStream

  • 1-Indanone
  • 2,3-Dihydro-1H-inden-1-ol

Customs

[ HS Code ]: 2906299090

[ Summary ]:
2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Naturally occurring variants of human aldo-keto reductases with reduced in vitro metabolism of daunorubicin and doxorubicin.

J. Pharmacol. Exp. Ther. 335 , 533-545, (2010)

Doxorubicin (DOX) and daunorubicin (DAUN) are effective anticancer drugs; however, considerable interpatient variability exists in their pharmacokinetics. This may be caused by altered metabolism by n...

Stereochemical sensitivity of the human UDP-glucuronosyltransferases 2B7 and 2B17.

J. Med. Chem. 49 , 1818-27, (2006)

A set of 28 enantiomers comprising rigid and flexible secondary alcohols was synthesized by the asymmetric Corey-Bakshi-Shibata reduction. The enantiomerically pure alcohols were subjected to enzymati...

Determination of the single component and competitive adsorption isotherms of the 1-indanol enantiomers by the inverse method.

J. Chromatogr. A. 1005(1-2) , 35-49, (2003)

The inverse method of isotherm determination consists in calculating the numerical values of the coefficients of an isotherm model that give a set of chromatographic profiles in best possible agreemen...


More Articles


Related Compounds

  • (R)-1-Amino-indan-4-ol hydrochloride
  • (R)-1,1,1-trichloro-4-phenylbutan-2-ol
  • (R)-1-TERT-BUTOXY-2-PROPANOL
  • (R)-1-benzyl-3-fluoro-piperidine
  • (R)-1-(4-(METHYLSULFONYL)PHENYL)ETHANAMINE
  • r-1-iodo-c-4-t-butyl-1-thiocyanatomethylcyclohexane
  • Benzyl 5-bromo-6-fluoro-1,2,3,4-tetrahydroisoquinoline-2-carboxylate
  • Benzyl 8-bromo-7-fluoro-1,2,3,4-tetrahydroisoquinoline-2-carboxylate
  • Benzyl 6-bromo-8-fluoro-1,2,3,4-tetrahydroisoquinoline-2-carboxylate
  • tert-butyl N-(4-bromo-2,6-dimethylphenyl)-N-(2,2-difluoroethyl)carbamate
  • 2-(3,4-dihydro-2H-1-benzopyran-8-yl)butanoic acid
  • benzyl N-[3-(4-bromophenyl)-2-hydroxypropyl]carbamate
  • benzyl N-(5-bromo-4-cyano-2-nitrophenyl)carbamate
  • benzyl N-(6-bromo-8-fluoroquinazolin-4-yl)carbamate
  • benzyl N-(6-bromo-4-oxo-3,4-dihydro-2H-1-benzopyran-3-yl)carbamate
  • benzyl N-(2-{6-bromo-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl}ethyl)carbamate
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