1-benzyl-2,3-dihydro-1H-indol-5-amine

Base Information

Chemical Name:1-benzyl-2,3-dihydro-1H-indol-5-amine
CAS No.:21909-45-5
Molecular Formula:C15H16N2
Molecular Weight:224.305
Hs Code.:2933990090
DSSTox Substance ID:DTXSID30655704
Nikkaji Number:J83.114J
Wikidata:Q82569930
Mol file:21909-45-5.mol

Synonyms:1-benzyl-2,3-dihydro-1H-indol-5-amine;21909-45-5;5-Amino-1-benzylindoline;1-BENZYL-2,3-DIHYDROINDOL-5-AMINE;1-benzylindolin-5-amine;SCHEMBL7476041;DTXSID30655704;AKOS000223912;FT-0745180;EN300-53328

Suppliers and Price of 1-benzyl-2,3-dihydro-1H-indol-5-amine

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

Labseeker
1H-INDOL-5-AMINE,2,3-DIHYDRO-1-(PHENYLMETHYL)- 95
5g
$ 1417.00

Labseeker
1H-INDOL-5-AMINE,2,3-DIHYDRO-1-(PHENYLMETHYL)- 95
10g
$ 1767.00

American Custom Chemicals Corporation
1H-INDOL-5-AMINE,2,3-DIHYDRO-1-(PHENYLMETHYL)- 95.00%
5G
$ 1759.28

American Custom Chemicals Corporation
1H-INDOL-5-AMINE,2,3-DIHYDRO-1-(PHENYLMETHYL)- 95.00%
2.5G
$ 1363.65

American Custom Chemicals Corporation
1H-INDOL-5-AMINE,2,3-DIHYDRO-1-(PHENYLMETHYL)- 95.00%
1G
$ 925.31

Total 2 raw suppliers

Chemical Property of 1-benzyl-2,3-dihydro-1H-indol-5-amine

Chemical Property:

PSA：29.26000
LogP:3.47770
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:224.131348519
Heavy Atom Count:17
Complexity:247

Purity/Quality:

98% ^*data from raw suppliers

1H-INDOL-5-AMINE,2,3-DIHYDRO-1-(PHENYLMETHYL)- 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(C2=C1C=C(C=C2)N)CC3=CC=CC=C3

Technology Process of 1-benzyl-2,3-dihydro-1H-indol-5-amine

There total 5 articles about 1-benzyl-2,3-dihydro-1H-indol-5-amine 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: 91.0%

: 227956-83-4
1-benzyl-5-nitro-2,3-dihydro-1H-indole

: 21909-45-5
1-benzyl-2,3-dihydro-1H-indol-5-ylamine

Guidance literature:: With iron; ammonium chloride; In ethanol; for 3h; Heating;
DOI:10.1021/jm040159c

Reference yield:

: 32692-19-6
5-nitro-2,3-dihydro-1H-indole

: 21909-45-5
1-benzyl-2,3-dihydro-1H-indol-5-ylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / acetonitrile / 2 h / Heating

2: 91 percent / iron; aq. NH₄Cl / ethanol / 3 h / Heating

With iron; ammonium chloride; In ethanol; acetonitrile;
DOI:10.1021/jm040159c

Reference yield:

: 100-39-0
benzyl bromide

: 21909-45-5
1-benzyl-2,3-dihydro-1H-indol-5-ylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / acetonitrile / 2 h / Heating

2: 91 percent / iron; aq. NH₄Cl / ethanol / 3 h / Heating

With iron; ammonium chloride; In ethanol; acetonitrile;
DOI:10.1021/jm040159c