9H-Carbazol-4-amine

Base Information

Chemical Name:9H-Carbazol-4-amine
CAS No.:18992-64-8
Molecular Formula:C12H10 N2
Molecular Weight:182.225
Hs Code.:2933990090
DSSTox Substance ID:DTXSID50172423
Nikkaji Number:J83.321E
Wikidata:Q72439173
Mol file:18992-64-8.mol

Synonyms:9H-Carbazol-4-amine;4-Aminocarbazole;18992-64-8;Carbazol-4-amine;SCHEMBL3433644;DTXSID50172423;AKOS006370990;N13363;A853247

Suppliers and Price of 9H-Carbazol-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

Crysdot
9H-Carbazol-4-amine 95+%
1g
$ 880.00

AccelPharmtech
9H-Carbazol-4-amine 97.00%
25G
$ 8830.00

AccelPharmtech
9H-Carbazol-4-amine 97.00%
5G
$ 3570.00

AccelPharmtech
9H-Carbazol-4-amine 97.00%
1G
$ 2080.00

Total 7 raw suppliers

Chemical Property of 9H-Carbazol-4-amine

Chemical Property:

Vapor Pressure:5.75E-08mmHg at 25°C
Melting Point:>300℃
Boiling Point:440.8°Cat760mmHg
Flash Point:250.6°C
PSA：41.81000
Density:1.317g/cm³
LogP:3.48450
XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:182.084398327
Heavy Atom Count:14
Complexity:216

Purity/Quality:

97% ^*data from raw suppliers

9H-Carbazol-4-amine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C3=C(C=CC=C3N2)N

Technology Process of 9H-Carbazol-4-amine

There total 11 articles about 9H-Carbazol-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: 65.0%

: 1454-80-4
1,1'-biphenyl-2,2'-diamine

: 18992-64-8
4-aminocarbazole

: 86-74-8,105184-46-1,97960-57-1
9H-carbazole

Guidance literature:: With calcium oxide; at 560 ℃; for 0.666667h;
DOI:10.1002/jhet.5570410101

Reference yield: 30.0%

: 52602-39-8
9H-carbazol-4-ol

: 18992-64-8
4-aminocarbazole

Guidance literature:: With sodium tetrahydroborate; 5%-palladium/activated carbon; hydrazine hydrate; In 1,4-dioxane; at 170 ℃; for 16h; Molecular sieve; Inert atmosphere;
DOI:10.1039/c9sc00595a