methyl-1-pentyl-1H-indole-3-Carboxylate

Base Information

Chemical Name:methyl-1-pentyl-1H-indole-3-Carboxylate
CAS No.:1338925-20-4
Molecular Formula:C15H19NO2
Molecular Weight:245.321
Hs Code.:
Mol file:1338925-20-4.mol

Synonyms:methyl-1-pentyl-1H-indole-3-Carboxylate

Suppliers and Price of methyl-1-pentyl-1H-indole-3-Carboxylate

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

Cayman Chemical
methyl-1-pentyl-1H-indole-3-Carboxylate ≥98%
10mg
$ 350.00

Cayman Chemical
methyl-1-pentyl-1H-indole-3-Carboxylate ≥98%
5mg
$ 225.00

Cayman Chemical
methyl-1-pentyl-1H-indole-3-Carboxylate ≥98%
1mg
$ 95.00

AK Scientific
Methyl1-pentyl-1H-indole-3-carboxylate
5mg
$ 403.00

Total 9 raw suppliers

Chemical Property of methyl-1-pentyl-1H-indole-3-Carboxylate

Chemical Property:

PSA：31.23000
LogP:3.61810

Purity/Quality:

99% ^*data from raw suppliers

methyl-1-pentyl-1H-indole-3-Carboxylate ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description PB-22 is synthetic cannabinoid that has been identified in herbal mixtures. It is a quinolinyl pentyl indole with a carboxylate group, abbreviated as QUPIC. methy-1-pentyl-1H-indole-3-Carboxylate is an analog of PB-22 that lacks the quinoline group. The physiological and toxicological properties of methyl-1-pentyl-1H-indole-3-Carboxylate are not known. This product is intended for forensic and research applications.

Technology Process of methyl-1-pentyl-1H-indole-3-Carboxylate

There total 1 articles about methyl-1-pentyl-1H-indole-3-Carboxylate 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: 58.0%

: 942-24-5
3-methoxycarbonylindole

: 110-53-2
1-Bromopentane

: 1338925-20-4
methyl 1-pentyl-1H-indole-3-carboxylate

Guidance literature:: 3-methoxycarbonylindole; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 0.5h; Inert atmosphere;

1-Bromopentane; In N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1016/j.ejmech.2011.08.021

Reference yield: 92.0%

: 1338925-20-4
methyl 1-pentyl-1H-indole-3-carboxylate

: 727421-73-0
1-pentyl-1H-indole-3-carboxylic acid

Guidance literature:: methyl 1-pentyl-1H-indole-3-carboxylate; With potassium hydroxide; In ethanol; water; at 20 - 75 ℃;

With hydrogenchloride; In ethanol; water;
DOI:10.1016/j.ejmech.2011.08.021

Reference yield: 85.0%

: 1338925-20-4
methyl 1-pentyl-1H-indole-3-carboxylate

: 134-32-7
1-amino-naphthalene

: 1338925-11-3
N-(naphthalen-1-yl)-1-pentyl-1H-indole-3-carboxamide

Guidance literature:: 1-amino-naphthalene; With trimethylaluminum; In 1,2-dichloro-ethane; toluene; at 20 ℃; for 0.166667h; Inert atmosphere;

methyl 1-pentyl-1H-indole-3-carboxylate; In 1,1,1-trichloroethane; toluene; for 24h; Inert atmosphere; Reflux;
DOI:10.1016/j.ejmech.2011.08.021