(+)-Bicifadine Hydrochloride

Base Information

Chemical Name:(+)-Bicifadine Hydrochloride
CAS No.:66504-82-3
Molecular Formula:C12H16ClN
Molecular Weight:209.719
Hs Code.:

Synonyms:(1R,5S)-1-(4-Methylphenyl)-

Suppliers and Price of (+)-Bicifadine 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

TRC
(+)-BicifadineHydrochloride
50mg
$ 1230.00

Chemenu
(1R,5S)-1-(p-tolyl)-3-azabicyclo[3.1.0]hexanehydrochloride 95%
500mg
$ 593.00

Biosynth Carbosynth
(+)-Bicifadine hydrochloride
50 mg
$ 1529.00

Biosynth Carbosynth
(+)-Bicifadine hydrochloride
25 mg
$ 841.00

Biosynth Carbosynth
(+)-Bicifadine hydrochloride
10 mg
$ 462.50

Biosynth Carbosynth
(+)-Bicifadine hydrochloride
5 mg
$ 254.40

Biosynth Carbosynth
(+)-Bicifadine hydrochloride
2 mg
$ 139.90

Total 4 raw suppliers

Chemical Property of (+)-Bicifadine Hydrochloride

Chemical Property:

PSA：12.03000
LogP:2.98670

Purity/Quality:

99% ^*data from raw suppliers

(+)-BicifadineHydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (+)-Bicifadine Hydrochloride

There total 4 articles about (+)-Bicifadine 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: 87.0%

: 83213-66-5
(1R,5S)-1-(4-methylphenyl)-3-azabicyclo[3.1.0]hexane

: 66504-82-3
(1R,5S)-1-(4-methylphenyl)-3-azabicyclo<3.1.0>hexane hydrochloride

Guidance literature:: With hydrogenchloride; In ethyl acetate; isopropyl alcohol; at 20 ℃; Product distribution / selectivity;

Reference yield: 66.0%

: (1R,2S)-2-(benzyloxymethyl)-1-p-tolylcyclopropanecarbonitrile

: 66504-82-3
(1R,5S)-1-(4-methylphenyl)-3-azabicyclo<3.1.0>hexane hydrochloride

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 175 ℃; Inert atmosphere; Microwave irradiation;
DOI:10.1021/jo302443k

Reference yield:

: C₁₁H₁₄ClN

: 66504-82-3
(1R,5S)-1-(4-methylphenyl)-3-azabicyclo<3.1.0>hexane hydrochloride

Guidance literature:: C₁₁H₁₄ClN; With sodium hydroxide; In Isopropyl acetate; water; at 30 ℃; for 3 - 5h; pH=8.5 - 9.0;

With hydrogenchloride; In Isopropyl acetate; water; at 30 ℃;