(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol structure
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Common Name | (1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol | ||
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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 |
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. |
Name | (1R,2S)-(+)-1-Amino-2-Hydroxyindan |
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Synonym | More Synonyms |
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. |
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Related Catalog |
Density | 1.2±0.1 g/cm3 |
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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 |
Symbol |
GHS07 |
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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 |
~33% (1R,2S)-1-Amino... CAS#:136030-00-7 |
Literature: Sakurai, Rumiko; Sakai, Kenichi Tetrahedron Asymmetry, 2003 , vol. 14, # 4 p. 411 - 413 |
Precursor 1 | |
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DownStream 2 | |
HS Code | 2922199090 |
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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% |
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... |
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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... |
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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... |
(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 |