(1R,2S)-1-amino-2-indanol

Base Information Edit

Chemical Name:(1R,2S)-1-amino-2-indanol
CAS No.:136030-00-7
Molecular Formula:C9H11NO
Molecular Weight:149.192
Hs Code.:29061990
European Community (EC) Number:422-660-2,603-940-5
UNII:71S3J7NU1B,7ZP212ZC8J
Nikkaji Number:J655.022C
ChEMBL ID:CHEMBL4546964
Mol file:136030-00-7.mol

Synonyms:136030-00-7;(1R,2S)-1-amino-2-indanol;(1R,2S)-1-amino-2,3-dihydro-1H-inden-2-ol;cis-1-Amino-2-indanol;7480-35-5;(1R,2S)-(+)-cis-1-Amino-2-indanol;cis-1-Amino-2,3-dihydro-1H-inden-2-ol;140632-20-8;13630-00-7;1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1R,2S)-;1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1R,2S)-rel-;(1R,2S)-(+)-1-Amino-2-indanol;Cis-1-Amino-2-hydroxyindan;71S3J7NU1B;7ZP212ZC8J;1-Amino-2-indanol, cis-(+)-;(1r,2s)-cis-1-amino-2-indanol;1-Amino-2-indanol, cis-(+/-)-;EC 422-660-2;(1R,2S)-2,3-Dihydro-2-hydroxyinden-1-ylamine;(1R,2S)-(+)-1-Amino-2-hydroxyindan;MFCD00216656;(1r,2s)-(+)-cis-1-aminoindan-2-ol;RAC-AMINDA;cis 1-amino-2-indanol;cis-1 -amino-2-indanol;1beta-Aminoindan-2beta-ol;UNII-71S3J7NU1B;UNII-7ZP212ZC8J;(1R,2S)-amino-2-indanol;SCHEMBL163842;Racemic cis-1-amino-2-indanol;CHEMBL4546964;1-(R)-amino-2-(S)-indanol;(1R,2S)-1-Aminoindan-2-ol;cis-(+/-)-1-aminoindan-2-ol;Cis-(-)-1-Amino-indane-2-ol;LOPKSXMQWBYUOI-DTWKUNHWSA-N;(1R,2S)-1-amino-indan-2-ol;cis-(1r,2s)-1-amino-2-indanol;cis-(1R,2S)-l-amino-2-indanol;(1R, 2S)-1-amino-indan-2-ol;(1R,2S)-1-Amino-2-hydroxyindan;(1r, 2s)-cis-1-amino-2-indanol;cis-1-Amino-2-indanol, AldrichCPR;MFCD01318239;AKOS005255542;AC-4656;CS-W007401;PS-4272;(1R, 2S)-(+)-1-amino-2-indanol;(1R,2S)-(-)-cis-1-Aminoindan-2-ol;BP-10106;(1r, 2s)-(+)-cis-1-amino-2-indanol;(1R,2S) -(+)-cis-1-amino-2-indanol;(1R,2S)-(-)-2-hydroxy-indan-1-ylamine;AM20060504;(1R,2S)-(+)-cis-1-Amino-2-hydroxyindane;EN300-53073;P15222;(1R,2S)-(+)-cis-1-Amino-2-indanol, 99%;A885809;A915553;rel-(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol;W-201145;1H-Inden-2-ol,1-amino-2,3-dihydro-, (1R,2S)-rel-;Z784894996;97-03-0

Suppliers and Price of (1R,2S)-1-amino-2-indanol

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(1R,2S)-1-Amino-2-indanol
500mg
$ 60.00

TRC
(1R,2S)-1-Amino-2-indanol
2.5g
$ 75.00

TRC
(1R,2S)-1-Amino-2-indanol
250mg
$ 45.00

TCI Chemical
(1R,2S)-(+)-1-Amino-2-indanol >98.0%(GC)(T)
5g
$ 42.00

TCI Chemical
(1R,2S)-(+)-1-Amino-2-indanol >98.0%(GC)(T)
1g
$ 14.00

SynQuest Laboratories
(1R,2S)-1-Amino-2-hydroxyindane
5 g
$ 23.00

Strem Chemicals
(1R,2S)-(+)-cis-1-Aminoindan-2-ol, 98%
1g
$ 27.00

Strem Chemicals
(1R,2S)-(+)-cis-1-Aminoindan-2-ol, 98%
5g
$ 108.00

Strem Chemicals
(1R,2S)-(+)-cis-1-Aminoindan-2-ol, 98%
25g
$ 432.00

Sigma-Aldrich
(1R,2S)-(+)-cis-1-Amino-2-indanol 99%
5g
$ 137.00

Total 114 raw suppliers

Chemical Property of (1R,2S)-1-amino-2-indanol Edit

Chemical Property:

Appearance/Colour:white to light yellow crystal powder
Vapor Pressure:0.001mmHg at 25°C
Melting Point:118-121 °C(lit.)
Refractive Index:43 ° (C=1, MeOH)
Boiling Point:290 ºC at 760 mmHg
PKA:14.79±0.40(Predicted)
Flash Point:129.2 ºC
PSA：46.25000
Density:1.212 g/cm³
LogP:1.30370
Storage Temp.:Keep in dark place,Inert atmosphere,Room temperature
Solubility.:soluble in Methanol
Water Solubility.:soluble
XLogP3:0.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:149.084063974
Heavy Atom Count:11
Complexity:149

Purity/Quality:

99% ^*data from raw suppliers

(1R,2S)-1-Amino-2-indanol ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn,Xi
Hazard Codes:Xi,Xn
Statements: 36/37/38-20/21/22
Safety Statements: 26-36-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(C2=CC=CC=C21)N)O
Isomeric SMILES:C1[C@@H]([C@@H](C2=CC=CC=C21)N)O
Uses (1R,2S)-1-Amino-2-indanol??Class of catalytic ligands which when used with a reducing agent, exhibit enantioselectivity in the reduction of a wide range of substrates. This cis-aminoindanol and its antipode have been used in the preparation of a series of potent HIV-1 protease inhibitory peptides. Also, they have served as chiral ligands in the catalytic asymmetric reduction of prochiral ketones with boranes.

Technology Process of (1R,2S)-1-amino-2-indanol

There total 133 articles about (1R,2S)-1-amino-2-indanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.3%