1-[Amino(phenyl)methyl]cyclohexan-1-ol

Base Information

Chemical Name:1-[Amino(phenyl)methyl]cyclohexan-1-ol
CAS No.:102729-78-2
Molecular Formula:C13H19NO
Molecular Weight:205.3
Hs Code.:
DSSTox Substance ID:DTXSID70544406
Mol file:102729-78-2.mol

Synonyms:102729-78-2;1-[Amino(phenyl)methyl]cyclohexan-1-ol;1-[amino(phenyl)methyl]cyclohexanol;1-(Amino(phenyl)methyl)cyclohexanol;SCHEMBL7101907;DTXSID70544406;EN300-1641244

Suppliers and Price of 1-[Amino(phenyl)methyl]cyclohexan-1-ol

Supply Marketing:

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

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Chemical Property of 1-[Amino(phenyl)methyl]cyclohexan-1-ol

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:205.146664230
Heavy Atom Count:15
Complexity:193

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)(C(C2=CC=CC=C2)N)O

Technology Process of 1-[Amino(phenyl)methyl]cyclohexan-1-ol

There total 4 articles about 1-[Amino(phenyl)methyl]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: 88.0%

: 947-19-3
1-hydroxycyclohexyl phenyl ketone

: 102729-78-2
1-(α-Amino-benzyl)-cyclohexanol

Guidance literature:: With nickel(II) tetrafluoroborate hexahydrate; ammonia; hydrogen; bis(2-diphenylphosphinoethyl)phenylphosphine; In 2,2,2-trifluoroethanol; at 120 ℃; for 24h; chemoselective reaction;
DOI:10.1039/d0sc01084g

Reference yield:

: 24731-36-0
1-trimethylsilanyloxycyclohexanecarbonitrile

: 102729-78-2
1-(α-Amino-benzyl)-cyclohexanol

Guidance literature:: With sodium tetrahydroborate; Yield given. Multistep reaction; 1.) ether, r.t., overnight, 2.) MeOH, r.t., 4 h;
DOI:10.1055/s-1986-31590

Reference yield:

: 931-97-5
1-hydroxy-1-cyclohexanecarbonitrile

: 102729-78-2
1-(α-Amino-benzyl)-cyclohexanol

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether; hydrogen chloride

2: diethyl ether / und Erwaermen des Reaktionsprodukts mit LiAlH₄ in Aether

With hydrogenchloride; diethyl ether;