Indolin-4-amine

Base Information

Chemical Name:Indolin-4-amine
CAS No.:52537-01-6
Molecular Formula:C8H10N2
Molecular Weight:134.181
Hs Code.:2933998090
DSSTox Substance ID:DTXSID60456463
Nikkaji Number:J258.982F
Wikidata:Q82278964
Mol file:52537-01-6.mol

Synonyms:INDOLIN-4-AMINE;52537-01-6;2,3-dihydro-1H-indol-4-amine;4-AMINOINDOLINE;4-AMINO-2,3-DIHYDRO-1H-INDOLE;SCHEMBL126414;DTXSID60456463;MXXKDNVTCQXXHU-UHFFFAOYSA-N;1H-Indol-4-amine,2,3-dihydro-;MFCD08234591;AKOS006287427;MB05532;AS-56625;CS-0105948;FT-0692515;O11831;EN300-2978022;A870964;A903039;151981-24-7

Suppliers and Price of Indolin-4-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

TRC
Indolin-4-amine
100mg
$ 175.00

SynQuest Laboratories
2,3-Dihydro-1H-indol-4-amine 98%
5 g
$ 1159.00

SynQuest Laboratories
2,3-Dihydro-1H-indol-4-amine 98%
250 mg
$ 148.00

SynQuest Laboratories
2,3-Dihydro-1H-indol-4-amine 98%
1 g
$ 364.00

Crysdot
Indolin-4-amine 95+%
1g
$ 210.00

Crysdot
Indolin-4-amine 95+%
5g
$ 665.00

Chemenu
Indolin-4-amine 95%
1g
$ 374.00

Chemenu
Indolin-4-amine 95%
5g
$ 1122.00

Apolloscientific
2,3-Dihydro-1H-indol-4-amine
1g
$ 330.00

Apolloscientific
2,3-Dihydro-1H-indol-4-amine
250mg
$ 134.00

Total 18 raw suppliers

Chemical Property of Indolin-4-amine

Chemical Property:

PSA：38.05000
LogP:1.95600
Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C
XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:134.084398327
Heavy Atom Count:10
Complexity:124

Purity/Quality:

97% ^*data from raw suppliers

Indolin-4-amine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CNC2=CC=CC(=C21)N
Uses Indolin-4-amine is used in preparation of heterocycle derivative for therapy of hair loss.

Technology Process of Indolin-4-amine

There total 1 articles about Indolin-4-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:

: 118742-89-5
2-(2,6-diaminophenyl)ethanol

: 85926-99-4
4-hydroxyindoline

: 52537-01-6
4-aminoindoline

Guidance literature:: With phosphoric acid; at 220 ℃; for 24h; Product distribution; variation of concentration of H₃PO₄;
DOI:10.1246/bcsj.62.3742

Reference yield: 86.0%

: 52537-01-6
4-aminoindoline

: 85926-99-4
4-hydroxyindoline

Guidance literature:: With phosphoric acid; at 220 ℃; for 24h;
DOI:10.1246/bcsj.62.3742

Reference yield:

: 52537-01-6
4-aminoindoline

: 2380-94-1
1H-indol-4-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / aq. 30percent H₃PO₄ / 24 h / 220 °C

2: 88 percent / 10percent Pd/C / o-xylene / 2.3 h / Heating

With palladium on activated charcoal; phosphoric acid; In o-xylene;
DOI:10.1246/bcsj.62.3742