N-Benzyl(2-hydroxycyclopentyl)methanaminium

Base Information

Chemical Name:N-Benzyl(2-hydroxycyclopentyl)methanaminium
CAS No.:20520-98-3
Molecular Formula:C13H19 N O
Molecular Weight:206.3035
Hs Code.:2922199090
DSSTox Substance ID:DTXSID80942696
Mol file:20520-98-3.mol

Synonyms:DTXSID80942696;N-Benzyl(2-hydroxycyclopentyl)methanaminium;20520-98-3

Suppliers and Price of N-Benzyl(2-hydroxycyclopentyl)methanaminium

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

American Custom Chemicals Corporation
CIS-2-BENZYLAMINOMETHYL-1-CYCLOPENTANOL HYDROCHLORIDE 95.00%
5MG
$ 500.17

Total 8 raw suppliers

Chemical Property of N-Benzyl(2-hydroxycyclopentyl)methanaminium

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:164-166oC
Refractive Index:1.6330 (estimate)
Boiling Point:330.9°Cat760mmHg
Flash Point:112°C
PSA：32.26000
Density:g/cm³
LogP:3.13010
XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:206.154489261
Heavy Atom Count:15
Complexity:177

Purity/Quality:

98%Min ^*data from raw suppliers

CIS-2-BENZYLAMINOMETHYL-1-CYCLOPENTANOL HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 37/39-26

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(C(C1)O)C[NH2+]CC2=CC=CC=C2
Isomeric SMILES:C1C[C@H]([C@H](C1)O)C[NH2+]CC2=CC=CC=C2

Technology Process of N-Benzyl(2-hydroxycyclopentyl)methanaminium

There total 4 articles about N-Benzyl(2-hydroxycyclopentyl)methanaminium 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: 93.0%

: 20657-48-1,20657-49-2
cis-2-benzoylaminomethyl-1-cyclopentanol

: 20520-98-3
(1S,2S)-2-(Benzylamino-methyl)-cyclopentanol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 24h; Heating;

Reference yield:

: 6282-02-6
N-(hydroxymethyl)benzamide

: 20520-98-3
(1S,2S)-2-(Benzylamino-methyl)-cyclopentanol

Guidance literature:: Multi-step reaction with 3 steps

1: 64 percent / conc. sulfuric acid / acetic acid / 4 h / 12 - 15 °C

2: 85 percent / 20 percent NaOH / ethanol; H₂O / 18 h / Heating

3: 93 percent / lithium tetrahydridoaluminate(III) / diethyl ether / 24 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; sulfuric acid; In diethyl ether; ethanol; water; acetic acid;

Reference yield:

: 97942-14-8
cis-2-phenyl-1,4,4a,5,6,7,7a-hexahydrocyclopenta[e][1,3]oxazine

: 20520-98-3
(1S,2S)-2-(Benzylamino-methyl)-cyclopentanol

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / 20 percent NaOH / ethanol; H₂O / 18 h / Heating

2: 93 percent / lithium tetrahydridoaluminate(III) / diethyl ether / 24 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; In diethyl ether; ethanol; water;