(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol

Modify Date: 2024-01-02 21:56:24

(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol Structure
(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol structure
Common Name (1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol
CAS Number 136030-00-7 Molecular Weight 149.19
Density 1.2±0.1 g/cm3 Boiling Point 290.0±40.0 °C at 760 mmHg
Molecular Formula C9H11NO Melting Point 117-121ºC
MSDS Chinese USA Flash Point 129.2±27.3 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of (1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol


(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.

 Names

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

  Biological Activity

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 Catalog

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 290.0±40.0 °C at 760 mmHg
Melting Point 117-121ºC
Molecular Formula C9H11NO
Molecular Weight 149.19
Flash Point 129.2±27.3 °C
Exact Mass 149.084061
PSA 46.25000
LogP 0.43
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.626

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn
Risk Phrases R20/21/22;R36/37/38
Safety Phrases S26-S36/37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922199090

 Customs

HS Code 2922199090
Summary 2922199090. 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