R-(+)-7-Hydroxy-DPAT hydrobromide

Base Information

Chemical Name:R-(+)-7-Hydroxy-DPAT hydrobromide
CAS No.:82730-72-1
Molecular Formula:C₁₆H₂₅NO
Molecular Weight:247.381
Hs Code.:2922299090
DSSTox Substance ID:DTXSID701017548
ChEMBL ID:CHEMBL1256389
Mol file:82730-72-1.mol

Synonyms:R-(+)-7-Hydroxy-DPAT hydrobromide;82730-72-1;EU-0100569;CHEMBL1256389;DPAT, (R)-7-OH-;DTXSID701017548;Tox21_500569;CCG-221873;LP00569;NCGC00093953-01;NCGC00261254-01;H-168;1021878-34-1;R(+)-7-Hydroxy-dipropylaminotetralin hydrobromide;SR-01000075926;SR-01000075926-1;(7R)-7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-2-ol;hydrobromide;(R)-7-Dipropylamino-5,6,7,8-tetrahydro-naphthalen-2-ol hydrobromide

Suppliers and Price of R-(+)-7-Hydroxy-DPAT hydrobromide

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

American Custom Chemicals Corporation
(R)-(+) 7-HYDROXY-DPAT 95.00%
25MG
$ 1009.62

American Custom Chemicals Corporation
(R)-(+) 7-HYDROXY-DPAT 95.00%
5MG
$ 320.10

Total 4 raw suppliers

Chemical Property of R-(+)-7-Hydroxy-DPAT hydrobromide

Chemical Property:

PSA：23.47000
LogP:3.37150
Solubility.:H2O: >100 mg/mL
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:327.11978
Heavy Atom Count:19
Complexity:237

Purity/Quality:

95% ^*data from raw suppliers

(R)-(+) 7-HYDROXY-DPAT 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCN(CCC)C1CCC2=C(C1)C=C(C=C2)O.Br
Isomeric SMILES:CCCN(CCC)[C@@H]1CCC2=C(C1)C=C(C=C2)O.Br

Technology Process of R-(+)-7-Hydroxy-DPAT hydrobromide

There total 3 articles about R-(+)-7-Hydroxy-DPAT hydrobromide 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:

: 158111-39-8
(R)-7-OMe-DPAT

: 82730-72-1
R-(+)-7-hydroxy-2-dipropylaminotetraline

Guidance literature:: With boron tribromide; In dichloromethane; Ambient temperature;
DOI:10.1021/jm00380a012

Reference yield:

: 93503-15-2,136655-71-5
N-((R)-7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-N-propyl-propionamide

: 82730-72-1
R-(+)-7-hydroxy-2-dipropylaminotetraline

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄ / diethyl ether

2: BBr₃ / CH₂Cl₂ / Ambient temperature

With lithium aluminium tetrahydride; boron tribromide; In diethyl ether; dichloromethane;
DOI:10.1021/jm00380a012

Reference yield:

: 93503-08-3
(R)-7-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amine hydrochloride

: 82730-72-1
R-(+)-7-hydroxy-2-dipropylaminotetraline

Guidance literature:: Multi-step reaction with 3 steps

1: 5percent aq. NaOH / 0.5 h

2: LiAlH₄ / diethyl ether

3: BBr₃ / CH₂Cl₂ / Ambient temperature

With sodium hydroxide; lithium aluminium tetrahydride; boron tribromide; In diethyl ether; dichloromethane;
DOI:10.1021/jm00380a012