Quinuclidin-3-yldi(thiophen-2-yl)methanol hydrochloride

Base Information

Chemical Name:Quinuclidin-3-yldi(thiophen-2-yl)methanol hydrochloride
CAS No.:57734-76-6
Molecular Formula:C16H20ClNOS2
Molecular Weight:341.9191
Hs Code.:2934999090
DSSTox Substance ID:DTXSID20973323
Mol file:57734-76-6.mol

Synonyms:(quinuclidyl-3)-di-(thienyl-2)carbinol hydrochloride;quiditene

Suppliers and Price of Quinuclidin-3-yldi(thiophen-2-yl)methanol 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

Matrix Scientific
1-Azabicyclo[2.2.2]oct-3-yl(di-2-thienyl)methanolhydrochloride
500mg
$ 199.00

Crysdot
Quinuclidin-3-yldi(thiophen-2-yl)methanolhydrochloride 95+%
5g
$ 704.00

Aronis compounds
1-azabicyclo[2.2.2]oct-3-yl(di-2-thienyl)methanolhydrochloride
10g
$ 511.00

Arctom
Quinuclidin-3-yldi(thiophen-2-yl)methanolhydrochloride ≥95%
1g
$ 200.00

Alichem
Quinuclidin-3-yldi(thiophen-2-yl)methanolhydrochloride
5g
$ 696.78

AK Scientific
1-Azabicyclo[2.2.2]oct-3-yl(di-2-thienyl)methanolhydrochloride
500mg
$ 318.00

Total 9 raw suppliers

Chemical Property of Quinuclidin-3-yldi(thiophen-2-yl)methanol hydrochloride

Chemical Property:

Vapor Pressure:1.31E-08mmHg at 25°C
Boiling Point:442.5°Cat760mmHg
Flash Point:221.4°C
PSA：79.95000
Density:g/cm³
LogP:4.12720
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:341.0674843
Heavy Atom Count:21
Complexity:340

Purity/Quality:

97% ^*data from raw suppliers

1-Azabicyclo[2.2.2]oct-3-yl(di-2-thienyl)methanolhydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN2CCC1C(C2)C(C3=CC=CS3)(C4=CC=CS4)O.Cl

Technology Process of Quinuclidin-3-yldi(thiophen-2-yl)methanol hydrochloride

There total 2 articles about Quinuclidin-3-yldi(thiophen-2-yl)methanol 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: 67.4%

: 188290-36-0,8014-23-1,25233-34-5
thiophene

: 108-86-1,52753-63-6
bromobenzene

: 6238-33-1
3-quinuclidinecarboxylic acid ethyl ester

: 591-51-5
phenyllithium

: 57734-76-6
quiditene

Guidance literature:: bromobenzene; With lithium; In diethyl ether; for 1h; Heating;

thiophene; phenyllithium; at 25 ℃; for 0.75h;

3-quinuclidinecarboxylic acid ethyl ester; In diethyl ether; at -10 - -5 ℃; for 0.5h;
DOI:10.1007/BF02465745

Reference yield: 67.0%

: 188290-36-0,8014-23-1,25233-34-5
thiophene

: 108-86-1,52753-63-6
bromobenzene

: 6238-33-1
3-quinuclidinecarboxylic acid ethyl ester

: 57734-76-6
quiditene

Guidance literature:: bromobenzene; With lithium; In diethyl ether; for 1h; Heating;

thiophene; In diethyl ether; at 20 ℃; for 1.5h;

3-quinuclidinecarboxylic acid ethyl ester; With hydrogenchloride; In diethyl ether; water; at -10 - 20 ℃; for 1.5h;