CAS 136030-00-7|(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol

Introduction:Basic information about CAS 136030-00-7|(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol
CAS Number136030-00-7Molecular Weight149.19
Density1.2±0.1 g/cm3Boiling Point290.0±40.0 °C at 760 mmHg
Molecular FormulaC9H11NOMelting Point117-121ºC
MSDSChineseUSAFlash Point129.2±27.3 °C
Symbol
GHS07
Signal WordWarning

Names

Name(1R,2S)-(+)-1-Amino-2-Hydroxyindan
SynonymMore Synonyms

BiologicalActivity

Description(1R,2S)-1-Amino-2-indanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others

Chemical & Physical Properties

Density1.2±0.1 g/cm3
Boiling Point290.0±40.0 °C at 760 mmHg
Melting Point117-121ºC
Molecular FormulaC9H11NO
Molecular Weight149.19
Flash Point129.2±27.3 °C
Exact Mass149.084061
PSA46.25000
LogP0.43
Vapour Pressure0.0±0.6 mmHg at 25°C
Index of Refraction1.626
InChIKeyLOPKSXMQWBYUOI-DTWKUNHWSA-N
SMILESNC1c2ccccc2CC1O

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXn
Risk PhrasesR20/21/22;R36/37/38
Safety PhrasesS26-S36/37/39
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2922199090

Customs

HS Code2922199090
Summary2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles10

More Articles
A series of potent HIV-1 protease inhibitors containing a hydroxyethyl secondary amine transition state isostere: synthesis, enzyme inhibition, and antiviral activity.

J. Med. Chem. 35 , 2525, (1992)

A series of HIV-1 protease inhibitors containing a novel hydroxyethyl secondary amine transition state isostere has been synthesized. The compounds exhibit a strong preference for the (R) stereochemis...

Synthesis and antiviral activity of a series of HIV-1 protease inhibitors with functionality tethered to the P1 or P1' phenyl substituents: X-ray crystal structure assisted design.

J. Med. Chem. 35 , 1685, (1992)

By tethering of a polar hydrophilic group to the P1 or P1' substituent of a Phe-based hydroxyethylene isostere, the antiviral potency of a series of HIV protease inhibitors was improved. The optimum e...

HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: an investigation into the role of the P1' side chain on structure-activity.

J. Med. Chem. 35 , 1702, (1992)

A systematic investigation was undertaken to determine the role of the P1' sidechain in a series of hydroxyethylene isostere based inhibitors of HIV-1 protease. Substitution and homologation of the be...

Synonyms

(1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol
(1R,2S)-1-Aminoindan-2-ol
MFCD00216656
(1R,2S)-(+)-cis-1-Amino-2-hydroxyindane
1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1R,2S)-
(1R,2S)-(+)-1-Amino-2-indanol
(1R,2S)-(+)-1-Amino-2-hydroxyindan
(1R,2S)-(+)-cis-1-amino-2-indanol
(1R,2S)-1-Amino-2-indanol
Cis-(1R,2S)-1-amino-2-indanol
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