Deptropine maleate

Base Information

Chemical Name:Deptropine maleate
CAS No.:15475-43-1
Molecular Formula:C27H31NO5
Molecular Weight:449.5387
Hs Code.:
UNII:N3Y78ZMW6Q
Wikidata:Q27284517

Synonyms:Deptropine maleate;UNII-N3Y78ZMW6Q;N3Y78ZMW6Q;3-alpha-((10,11-Dihydro-5H-dibenzo(a,d)cyclohepten-5-yl)oxy)tropane maleate;1-alpha-H,5-alpha-H-Tropane, 3-alpha-((10,11-dihydro-5H-dibenzo(a,d)cyclohepten-5-yl)oxy)-, maleate (1:1);15475-43-1;C23-H27-N-O.C4-H4-O4;DEPTROPINE MALEATE [MI];LS-157776;Q27284517;TROPANE, 3.ALPHA.-((10,11-DIHYDRO-5H-DIBENZO(A,D)CYCLOHEPTEN-5-YL)OXY)-, MALEATE;(Z)-but-2-enedioic acid;(1R,5S)-8-methyl-3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,11,13-hexaenyloxy)-8-azabicyclo[3.2.1]octane;1.ALPHA.H,5.ALPHA.H-TROPANE, 3.ALPHA.-((10,11-DIHYDRO-5H-DIBENZO(A,D)CYCLOHEPTEN-5-YL)OXY)-, MALEATE (1:1);8-AZABICYCLO(3.2.1)OCTANE, 3-((10,11-DIHYDRO-5H-DIBENZO(A,D)CYCLOHEPTEN-5-YL)OXY)-8-METHYL-, (3-ENDO)-, (2Z)-2-BUTENEDIOATE (1:1)

Suppliers and Price of Deptropine maleate

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

Total 0 raw suppliers

Chemical Property of Deptropine maleate

Chemical Property:

Vapor Pressure:3.7E-08mmHg at 25°C
Boiling Point:446.3°C at 760 mmHg
Flash Point:130.4°C
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:449.22022309
Heavy Atom Count:33
Complexity:546

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2CCC1CC(C2)OC3C4=CC=CC=C4CCC5=CC=CC=C35.C(=CC(=O)O)C(=O)O
Isomeric SMILES:CN1[C@@H]2CC[C@H]1CC(C2)OC3C4=CC=CC=C4CCC5=CC=CC=C35.C(=C\C(=O)O)\C(=O)O

Technology Process of Deptropine maleate

There total 4 articles about Deptropine maleate 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:

: 604-51-3
3α-((10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)oxy)-8-methyl-8-azabicyclo[3.2.1]octane

: 110-16-7,26099-09-2
maleic acid

: 15475-43-1
3α-((10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)oxy)-8-methyl-8-azabicyclo[3.2.1]octane maleate

Guidance literature:: In ethyl acetate;
DOI:10.1016/j.bmcl.2011.12.008

Reference yield:

: 1210-33-9
5-chlorodibenzosuberane

: 15475-43-1
3α-((10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)oxy)-8-methyl-8-azabicyclo[3.2.1]octane maleate

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 20 °C

2: ethyl acetate

In ethyl acetate; toluene;
DOI:10.1016/j.bmcl.2011.12.008

Reference yield:

: 120-29-6
3-tropanol

: 15475-43-1
3α-((10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)oxy)-8-methyl-8-azabicyclo[3.2.1]octane maleate

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 20 °C

2: ethyl acetate

In ethyl acetate; toluene;
DOI:10.1016/j.bmcl.2011.12.008