(1R,2R)-2-(Benzyloxy)cyclohexanamine

Base Information Edit

Chemical Name:(1R,2R)-2-(Benzyloxy)cyclohexanamine
CAS No.:216394-06-8
Molecular Formula:C₁₃H₁₉NO
Molecular Weight:205.3
Hs Code.:29221990
European Community (EC) Number:606-810-6,619-352-7
DSSTox Substance ID:DTXSID70474517
Wikidata:Q72442225
Mol file:216394-06-8.mol

Synonyms:(1R,2R)-2-(Benzyloxy)cyclohexanamine;216394-06-8;(1R,2R)-(-)-2-Benzyloxycyclohexylamine;(1R,2R)-2-benzyloxycyclohexylamine;(1R,2R)-2-phenylmethoxycyclohexan-1-amine;98454-43-4;(1R,2R)-2-(benzyloxy)cyclohexan-1-amine;trans-2-(benzyloxy)cyclohexanamine;(1R,2R)-trans-2-Benzyloxy-cyclohexylamine;MFCD01075752;rel-((1R,2R)-2-(Benzyloxy)cyclohexanamine);SCHEMBL354344;DTXSID70474517;NTHNRYLIXJZHRZ-CHWSQXEVSA-N;AKOS015915354;AM62759;Trans-2-(benzyloxy)cyclohexan-1-amine;DS-16226;CS-0077156;(1r-trans)-2-(phenylmethoxy)cyclohexaneamine;EN300-196799;EN300-254704;rac-(1R,2R)-2-(benzyloxy)cyclohexan-1-amine;(1R,2R)-trans-2-Benzyloxycyclohexylamine, 96%;A815563;Cyclohexanamine, 2-(phenylmethoxy)-, (1R,2R)-;A1-24350;J-014198;(1R)-trans-2-(Phenylmethoxy)cyclohexanamine, (1R,2R)-1-Amino-2-benzyloxycyclohexane;(1R,2R)-trans-2-Benzyloxycyclohexylamine, ChiPros(R), produced by BASF, 99%

Suppliers and Price of (1R,2R)-2-(Benzyloxy)cyclohexanamine

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,2R)-2-(Benzyloxy)cyclohexanamine
250mg
$ 45.00

Sigma-Aldrich
(1R,2R)-trans-2-Benzyloxycyclohexylamine 96%
1g
$ 115.00

Crysdot
(1R,2R)-2-(Benzyloxy)cyclohexanamine 97%
10g
$ 232.00

Chemenu
(1R,2R)-2-(Benzyloxy)cyclohexanamine 95+%
25g
$ 234.00

Chemenu
(1R,2R)-2-(Benzyloxy)cyclohexanamine 95+%
10g
$ 112.00

American Custom Chemicals Corporation
(1R,2R)-2-PHENYLMETHOXYCYCLOHEXAN-1-AMINE 95.00%
5MG
$ 498.84

Alfa Aesar
(1R,2R)-(-)-2-Benzyloxycyclohexylamine, ChiPros 98+%, ee 98%
1g
$ 43.70

Alfa Aesar
(1R,2R)-(-)-2-Benzyloxycyclohexylamine, ChiPros 98+%, ee 98%
5g
$ 149.00

AK Scientific
(1R,2R)-(-)-2-Benzyloxycyclohexylamine
10g
$ 290.00

AK Scientific
(1R,2R)-(-)-2-Benzyloxycyclohexylamine
25g
$ 585.00

Total 49 raw suppliers

Chemical Property of (1R,2R)-2-(Benzyloxy)cyclohexanamine Edit

Chemical Property:

Vapor Pressure:0.001mmHg at 25°C
Refractive Index:1.5275
Boiling Point:306.1°Cat760mmHg
PKA:9.80±0.70(Predicted)
Flash Point:133.2°C
PSA：35.25000
Density:1.03g/cm³
LogP:3.17340
Storage Temp.:2-8°C
Sensitive.:Air Sensitive
Solubility.:Difficult to mix.
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:205.146664230
Heavy Atom Count:15
Complexity:177

Purity/Quality:

98% ^*data from raw suppliers

(1R,2R)-2-(Benzyloxy)cyclohexanamine ^*data from reagent suppliers

Safty Information:

Pictogram(s): R34:Causes burns.;
Hazard Codes:Xn
Statements: 34-36/37/38-22
Safety Statements: 26-36/37/39-45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C(C1)N)OCC2=CC=CC=C2
Isomeric SMILES:C1CC[C@H]([C@@H](C1)N)OCC2=CC=CC=C2

Technology Process of (1R,2R)-2-(Benzyloxy)cyclohexanamine

There total 12 articles about (1R,2R)-2-(Benzyloxy)cyclohexanamine 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: 95.0%

: (±)-trans-N-benzyl-2-(benzyloxy)cyclohexan-1-amine

: 98454-42-3,98454-43-4,216394-07-9,216394-06-8
(±)-trans-2-(benzyloxy)cyclohexanamine

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; laccase from Trametes versicolor; oxygen; In aq. buffer; at 30 ℃; for 16h; pH=5; Reagent/catalyst; chemoselective reaction; Enzymatic reaction;
DOI:10.1039/c5gc00525f