5-Isopropylindoline

Base Information

Chemical Name:5-Isopropylindoline
CAS No.:65826-96-2
Molecular Formula:C11H15N
Molecular Weight:161.24300
Hs Code.:2933990090
DSSTox Substance ID:DTXSID90443326
Wikidata:Q82261082
Mol file:65826-96-2.mol

Synonyms:5-Isopropylindoline;65826-96-2;5-(2-Propyl)indoline;1H-Indole, 2,3-dihydro-5-(1-methylethyl)-;SCHEMBL1615697;DTXSID90443326;LCIJJWUQMXUQQI-UHFFFAOYSA-N;AKOS009132647;SB64508;5-(propan-2-yl)-2,3-dihydro-1H-indole;CS-0275352;EN300-696537

Suppliers and Price of 5-Isopropylindoline

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

Chemenu
5-Isopropylindoline 95%+
25g
$ 2597.00

Chemenu
5-Isopropylindoline 95%+
10g
$ 1559.00

Chemenu
5-Isopropylindoline 95%+
5g
$ 1039.00

Chemenu
5-Isopropylindoline 95%+
1g
$ 520.00

American Custom Chemicals Corporation
2,3-DIHYDRO-5-(1-METHYLETHYL)-1H-INDOLE 95.00%
5MG
$ 502.81

Alichem
5-Isopropylindoline
5g
$ 1474.00

Total 4 raw suppliers

Chemical Property of 5-Isopropylindoline

Chemical Property:

PSA：12.03000
LogP:2.91600
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:161.120449483
Heavy Atom Count:12
Complexity:153

Purity/Quality:

99% ^*data from raw suppliers

5-Isopropylindoline 95%+ ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C1=CC2=C(C=C1)NCC2

Technology Process of 5-Isopropylindoline

There total 5 articles about 5-Isopropylindoline 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: 84.0%

: 97820-51-4
5-(isopropyl)-1H-indole

: 65826-96-2
5-(2-Propyl)indoline

Guidance literature:: With sodium cyanoborohydride; acetic acid; for 3h; Ambient temperature;
DOI:10.1021/jm970741j

Reference yield:

: 496-15-1
1-indoline

: 67-63-0,8013-70-5
isopropyl alcohol

: 65826-96-2
5-(2-Propyl)indoline

: 122299-59-6
6-isopropylindoline

Guidance literature:: With sulfuric acid; at 60 ℃; Rate constant;
DOI:10.1007/BF00476202

Reference yield:

: 99-88-7
4-Isopropylaniline

: 65826-96-2
5-(2-Propyl)indoline

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / H₂ / 5percent Pd/C / ethanol / 18 h / 760 Torr

2: 22 percent / trifluoroacetic acid

3: 86 percent / K₂CO₃ / methanol / 1.5 h / 55 °C

4: 84 percent / glac. AcOH, sodium cyanoborohydride / 3 h / Ambient temperature

With hydrogen; sodium cyanoborohydride; potassium carbonate; acetic acid; trifluoroacetic acid; palladium on activated charcoal; In methanol; ethanol;
DOI:10.1021/jm970741j