(1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol

Base Information

Chemical Name:(1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol
CAS No.:189362-43-4
Molecular Formula:C9H17NO
Molecular Weight:155.24
Hs Code.:
European Community (EC) Number:825-169-5
DSSTox Substance ID:DTXSID70573155
Nikkaji Number:J2.867.104K
Wikidata:Q82461750
Mol file:189362-43-4.mol

Synonyms:189362-43-4;(1R,2R)-2-(Cyclopropylamino)cyclohexanol;(1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol;(1R,2R)-2-CYCLOPROPYLAMINO CYCLOHEXANOL;SCHEMBL7803984;DTXSID70573155;CFEAMNVUJMQGNK-RKDXNWHRSA-N;AKOS006309847;EN300-1234887;trans-N-(2-hydroxycyclohexyl)-N-cyclopropylamine;rac-(1R,2R)-2-(cyclopropylamino)cyclohexan-1-ol

Suppliers and Price of (1R,2R)-2-(Cyclopropylamino)cyclohexan-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
(1R,2R)-2-(Cyclopropylamino)cyclohexanol 95+%
1g
$ 880.00

Chemenu
(1R,2R)-2-(cyclopropylamino)cyclohexan-1-ol 95%
1g
$ 830.00

Total 5 raw suppliers

Chemical Property of (1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol

Chemical Property:

Boiling Point:261.8±33.0 °C(Predicted)
PKA:14.99±0.40(Predicted)
PSA：32.26000
Density:1.05±0.1 g/cm3(Predicted)
LogP:1.43280
Storage Temp.:2-8°C
XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:155.131014166
Heavy Atom Count:11
Complexity:134

Purity/Quality:

97% ^*data from raw suppliers

(1R,2R)-2-(Cyclopropylamino)cyclohexanol 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C(C1)NC2CC2)O
Isomeric SMILES:C1CC[C@H]([C@@H](C1)NC2CC2)O

Technology Process of (1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol

There total 5 articles about (1R,2R)-2-(Cyclopropylamino)cyclohexan-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: 100.0%

: 189362-41-2
(S)-Hydroxy-phenyl-acetic acid (1R,2R)-2-cyclopropylamino-cyclohexyl ester

: 189362-43-4
(1R,2R)-2-(cyclopropylamino)cyclohexan-1-ol

Guidance literature:: With potassium hydroxide; In ethanol;
DOI:10.1016/S0960-894X(98)00246-7

Reference yield: 38.0%

: C₉H₁₇NO

: 189362-43-4
(1R,2R)-2-(cyclopropylamino)cyclohexan-1-ol

Guidance literature:: C₉H₁₇NO; With (2E)-but-2-enedioic acid; In isopropyl alcohol; at 40 ℃;

With potassium hydroxide; In water;
DOI:10.1246/bcsj.20170369

Reference yield:

: 286-20-4
cyclohexene oxide

: 765-30-0
Cyclopropylamine

: 189362-42-3
(1S,2S)-2-Cyclopropylamino-cyclohexanol

: 189362-43-4
(1R,2R)-2-(cyclopropylamino)cyclohexan-1-ol

Guidance literature:: With soy polysaccharide Soyafibe S-DN; In water; toluene; at 40 ℃; for 26h; Reagent/catalyst; Temperature; stereoselective reaction; Catalytic behavior; Inert atmosphere;
DOI:10.1246/bcsj.20170369