2-Aminocyclopentanol hydrochloride

Base Information

Chemical Name:2-Aminocyclopentanol hydrochloride
CAS No.:31889-37-9
Molecular Formula:C₅H₁₁NO*ClH
Molecular Weight:137.609
Hs Code.:2906190090
European Community (EC) Number:802-170-9
Mol file:31889-37-9.mol

Synonyms:2-aminocyclopentanol hydrochloride;2-aminocyclopentan-1-ol hydrochloride;98137-42-9;31775-67-4;trans-2-Aminocyclopentanol hydrochloride;2-aminocyclopentan-1-ol;hydrochloride;31889-37-9;(1R,2R)-rel-2-Aminocyclopentanol hydrochloride;cis-(1S,2R)-2-Aminocyclopentanol Hydrochloride;2-?Aminocyclopentanol HCL;MFCD07370091;MFCD08704797;2-Aminocyclopentanol HCl;NALTREXONEHYDROCHLORIDE;Propiophenone, b,b-diphenyl-;SCHEMBL285953;2-aminocyclopentanolhydrochloride;ZFSXKSSWYSZPGQ-UHFFFAOYSA-N;MFCD14705642;2-hydroxycyclopentylamine hydrochloride;AKOS016367729;AB12529;AB30961;SB12318;SB12327;SB12329;5,6-Dihydrocyclopenta(b )thiophen-4-one;SY002754;SY002755;SY003862;SY003863;CIS-2-AMINO-CYCLOPENTANOLHYDROCHLORIDE;EN300-56908;Trans-(-)-2-aminocyclopentanol hydrochloride;(1R,2R)-2-aminocyclopentanol hydrochloride

Suppliers and Price of 2-Aminocyclopentanol hydrochloride

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

SynQuest Laboratories
cis-2-Aminocyclopentanol hydrochloride
1 g
$ 952.00

Crysdot
cis-2-Aminocyclopentanolhydrochloride 95+%
1g
$ 515.00

Chemenu
cis-2-Aminocyclopentanolhydrochloride 95%
1g
$ 281.00

Biosynth Carbosynth
cis-2-Amino-cyclopentanolHydrochloride
250 mg
$ 250.00

Biosynth Carbosynth
cis-2-Amino-cyclopentanolHydrochloride
500 mg
$ 400.00

American Custom Chemicals Corporation
CIS-2-AMINO-CYCLOPENTANOL HYDROCHLORIDE 95.00%
5MG
$ 503.72

AK Scientific
cis-2-Aminocyclopentanolhydrochloride
250mg
$ 387.00

Total 10 raw suppliers

Chemical Property of 2-Aminocyclopentanol hydrochloride

Chemical Property:

Melting Point:179-180 °C
PSA：46.25000
LogP:1.36080
Storage Temp.:Inert atmosphere,Room Temperature
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:137.0607417
Heavy Atom Count:8
Complexity:65.1

Purity/Quality:

97% ^*data from raw suppliers

cis-2-Aminocyclopentanol hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(C(C1)O)N.Cl
Uses (1R,2S)-2-Aminocyclopentanol, HCl

Technology Process of 2-Aminocyclopentanol hydrochloride

There total 4 articles about 2-Aminocyclopentanol hydrochloride 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:

: 16936-83-7,18721-47-6,33092-75-0
(+/-)-2-(4-nitro-phenyl)-(3ar,6ac)-4,5,6,6a-tetrahydro-3aH-cyclopentoxazole

: 31775-67-4,31889-37-9,33092-89-6,68327-04-8,68327-11-7,98137-42-9,137254-03-6
cis-aminotetrahydro-3-furanol hydrochloride

Guidance literature:: With hydrogenchloride; water;
DOI:10.1021/ja01161a089

Reference yield:

: 33092-86-3
trans-2-aminocyclopentanol

: 31775-67-4,31889-37-9,33092-89-6,68327-04-8,68327-11-7,98137-42-9,137254-03-6
cis-aminotetrahydro-3-furanol hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: H₂O; benzene; aq. NaOH solution

2: SOCl₂

3: water; HCl

With hydrogenchloride; sodium hydroxide; thionyl chloride; water; benzene;
DOI:10.1021/ja01161a089

Reference yield:

: 33092-88-5,100135-54-4
(+/-)-4-nitro-benzoic acid-(trans-2-hydroxy-cyclopentylamide)

: 31775-67-4,31889-37-9,33092-89-6,68327-04-8,68327-11-7,98137-42-9,137254-03-6
cis-aminotetrahydro-3-furanol hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂

2: water; HCl

With hydrogenchloride; thionyl chloride; water;
DOI:10.1021/ja01161a089