3,4-Dihydro-1-isopropylisoquinoline-7-carbaldehyde

Base Information

Chemical Name:3,4-Dihydro-1-isopropylisoquinoline-7-carbaldehyde
CAS No.:371220-31-4
Molecular Formula:C13H15NO
Molecular Weight:201.26400
Hs Code.:2933499090
DSSTox Substance ID:DTXSID70471324
Wikidata:Q82299813
Mol file:371220-31-4.mol

Synonyms:371220-31-4;3,4-DIHYDRO-1-ISOPROPYLISOQUINOLINE-7-CARBALDEHYDE;1-propan-2-yl-3,4-dihydroisoquinoline-7-carbaldehyde;1-ISOPROPYL-3,4-DIHYDROISOQUINOLINE-7-CARBALDEHYDE;AB3664;SCHEMBL5776978;DTXSID70471324;PWHOFJDGMLMNIH-UHFFFAOYSA-N;MFCD09909386;1-isopropyl-3,4-dihydro-7-isoquinolinecarbaldehyde;1-(Propan-2-yl)-3,4-dihydroisoquinoline-7-carbaldehyde

Suppliers and Price of 3,4-Dihydro-1-isopropylisoquinoline-7-carbaldehyde

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

Crysdot
1-Isopropyl-3,4-dihydroisoquinoline-7-carbaldehyde 95+%
5g
$ 1648.00

Crysdot
1-Isopropyl-3,4-dihydroisoquinoline-7-carbaldehyde 95+%
1g
$ 549.00

American Custom Chemicals Corporation
3,4-DIHYDRO-1-ISOPROPYLISOQUINOLINE-7-CARBALDEHYDE 95.00%
5MG
$ 501.64

Total 1 raw suppliers

Chemical Property of 3,4-Dihydro-1-isopropylisoquinoline-7-carbaldehyde

Chemical Property:

PSA：29.43000
LogP:1.93590
XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:201.115364102
Heavy Atom Count:15
Complexity:270

Purity/Quality:: 1-Isopropyl-3,4-dihydroisoquinoline-7-carbaldehyde 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C1=NCCC2=C1C=C(C=C2)C=O

Technology Process of 3,4-Dihydro-1-isopropylisoquinoline-7-carbaldehyde

There total 4 articles about 3,4-Dihydro-1-isopropylisoquinoline-7-carbaldehyde 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:

: 371220-28-9
7-bromo-1-isopropyl-3,4-dihydroisoquinoline

: 371220-31-4
1-isopropyl-3,4-dihydro-7-isoquinolinecarbaldehyde

Guidance literature:: With n-butyllithium; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 371220-28-9
7-bromo-1-isopropyl-3,4-dihydroisoquinoline

: 371220-31-4
1-isopropyl-3,4-dihydro-7-isoquinolinecarbaldehyde

Guidance literature:: With n-butyllithium; In tetrahydrofuran; at -78 ℃;
DOI:10.1016/j.bmcl.2004.10.026

Reference yield:

: 73918-56-6
4-Bromophenethylamine

: 371220-31-4
1-isopropyl-3,4-dihydro-7-isoquinolinecarbaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1.1: Et₃N

2.1: (COCl)2; FeCl₃ / CHCl₃

2.2: HCl

3.1: n-BuLi / tetrahydrofuran / -78 °C

With n-butyllithium; oxalyl dichloride; iron(III) chloride; triethylamine; In tetrahydrofuran; chloroform;
DOI:10.1016/j.bmcl.2004.10.026