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

Base Information

Chemical Name:(1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol
CAS No.:23337-80-6
Molecular Formula:C9H11 N O
Molecular Weight:149.19
Hs Code.:2922199090
European Community (EC) Number:874-882-8
Nikkaji Number:J36.231J
Mol file:23337-80-6.mol

Synonyms:(1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol;142678-92-0;23337-80-6;cis-2-Amino-2,3-dihydro-1H-inden-1-ol;(+/-)-Cis-2-amino-1-hydroxyindane;cis-2-aminoindanol;1H-Inden-1-ol, 2-amino-2,3-dihydro-, cis-;cis-1-Hydroxy-2-aminoindan;SCHEMBL1239150;(1R,2S)-2-Aminoindan-1-ol;(+/-) cis 2-amino-1-indanol;HRWCWYGWEVVDLT-DTWKUNHWSA-N;(R)-5-Phosphono-2-aminovaleric acid

Suppliers and Price of (1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol

Supply Marketing:

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

Crysdot
cis-2-Amino-2,3-dihydro-1H-inden-1-ol 95+%
100mg
$ 267.00

Crysdot
cis-2-Amino-2,3-dihydro-1H-inden-1-ol 95+%
250mg
$ 428.00

Crysdot
cis-2-Amino-2,3-dihydro-1H-inden-1-ol 95+%
1g
$ 1070.00

American Custom Chemicals Corporation
(+/-)-CIS-2-AMINO-1-HYDROXYINDANE 95.00%
5MG
$ 496.13

Alichem
cis-2-Amino-2,3-dihydro-1H-inden-1-ol
250mg
$ 444.96

Alichem
cis-2-Amino-2,3-dihydro-1H-inden-1-ol
100mg
$ 275.40

Total 5 raw suppliers

Chemical Property of (1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol

Chemical Property:

Boiling Point:296.9±40.0 °C(Predicted)
PKA:13.85±0.40(Predicted)
PSA：46.25000
Density:1.212±0.06 g/cm3(Predicted)
LogP:1.30370
XLogP3:0.5
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

cis-2-Amino-2,3-dihydro-1H-inden-1-ol 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(C2=CC=CC=C21)O)N
Isomeric SMILES:C1[C@@H]([C@@H](C2=CC=CC=C21)O)N

Technology Process of (1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol

There total 19 articles about (1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol 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:

: 171482-71-6
(1R,2R)-2-azido-2,3-dihydro-1H-inden-1-ol

: 13575-72-9,15028-16-7,23337-80-6,32151-02-3,64282-60-6,64282-61-7,94077-01-7,94077-46-0,142678-92-0
(1R,2R)-trans-2-amino-1-indanol

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; at 25 ℃;
DOI:10.1016/0957-4166(95)00192-R

Reference yield:

: cis-(1RS,2SR)-2-azido-2,3-dihydro-1H-inden-1-ol

: 13575-72-9,15028-16-7,23337-80-6,32151-02-3,64282-60-6,64282-61-7,94077-01-7,94077-46-0,142678-92-0
(1R,2R)-trans-2-amino-1-indanol

Guidance literature:: Multi-step reaction with 4 steps

1: 25 percent / hexane; diethyl ether / 96 h / 40 °C

2: Ph₃P, DIAD

3: MeONa / methanol; CH₂Cl₂

4: H₂ / Pd/C / ethanol / 25 °C

With di-isopropyl azodicarboxylate; hydrogen; sodium methylate; triphenylphosphine; palladium on activated charcoal; In methanol; diethyl ether; ethanol; hexane; dichloromethane;
DOI:10.1016/0957-4166(95)00192-R

Reference yield:

: 166942-30-9
(1S,2R)-2-azido-2,3-dihydro-1H-inden1-ol

: 13575-72-9,15028-16-7,23337-80-6,32151-02-3,64282-60-6,64282-61-7,94077-01-7,94077-46-0,142678-92-0
(1R,2R)-trans-2-amino-1-indanol

Guidance literature:: Multi-step reaction with 3 steps

1: Ph₃P, DIAD

2: MeONa / methanol; CH₂Cl₂

3: H₂ / Pd/C / ethanol / 25 °C

With di-isopropyl azodicarboxylate; hydrogen; sodium methylate; triphenylphosphine; palladium on activated charcoal; In methanol; ethanol; dichloromethane;
DOI:10.1016/0957-4166(95)00192-R