Dimoxamine, (S)-

Base Information

Chemical Name:Dimoxamine, (S)-
CAS No.:52881-88-6
Molecular Formula:C₁₃H₂₁NO₂
Molecular Weight:223.315
Hs Code.:
UNII:GCX99AS3NZ
ChEMBL ID:CHEMBL2110031
Nikkaji Number:J563.402D

Synonyms:Dimoxamine, (S)-;GCX99AS3NZ;UNII-GCX99AS3NZ;52881-88-6;Benzeneethanamine, alpha-ethyl-2,5-dimethoxy-4-methyl-, (S)-;SCHEMBL896149;CHEMBL2110031;BENZENEETHANAMINE, .ALPHA.-ETHYL-2,5-DIMETHOXY-4-METHYL-, (S)-

Suppliers and Price of Dimoxamine, (S)-

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
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Total 0 raw suppliers

Chemical Property of Dimoxamine, (S)-

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:223.157228913
Heavy Atom Count:16
Complexity:198

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(CC1=C(C=C(C(=C1)OC)C)OC)N
Isomeric SMILES:CC[C@@H](CC1=C(C=C(C(=C1)OC)C)OC)N

Technology Process of Dimoxamine, (S)-

There total 3 articles about Dimoxamine, (S)- 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:

: 52807-48-4
1,4-Dimethoxy-2-methyl-5-((E)-2-nitro-but-1-enyl)-benzene

: 52881-88-6
(S)-1-(2,5-Dimethoxy-4-methyl-benzyl)-propylamine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1021/jm00234a010

Reference yield:

: 4925-88-6
2,5-dimethoxy-4-methylbenzaldehyde

: 52881-88-6
(S)-1-(2,5-Dimethoxy-4-methyl-benzyl)-propylamine

Guidance literature:: Multi-step reaction with 2 steps

1: NH₄OAc / acetic acid

2: LiAlH₄ / tetrahydrofuran

With lithium aluminium tetrahydride; ammonium acetate; In tetrahydrofuran; acetic acid;
DOI:10.1021/jm00234a010

Reference yield:

: 24599-58-4
2,5-dimethoxy toluene

: 52881-88-6
(S)-1-(2,5-Dimethoxy-4-methyl-benzyl)-propylamine

Guidance literature:: Multi-step reaction with 3 steps

1: (i) POCl₃, (ii) /BRN= 2045336/

2: NH₄OAc / acetic acid

3: LiAlH₄ / tetrahydrofuran

With lithium aluminium tetrahydride; ammonium acetate; In tetrahydrofuran; acetic acid;
DOI:10.1021/jm00234a010