Cas no 104636-53-5 (1-Phenyl-9h-carbazole)

1-Phenyl-9h-carbazole structure

Product Name:1-Phenyl-9h-carbazole

CAS No:104636-53-5

MF:C₁₈H₁₃N

MW:243.3025

CID:4741671

PubChem ID:13497474

Update Time:2026-02-25

1-Phenyl-9h-carbazole Chemical and Physical Properties

Names and Identifiers

- 1-phenyl-9h-carbazole
- phenylcarbazole
- 9H-Carbazole, phenyl-
- CHEMBL455562
- SCHEMBL191031
- G86133
- 96125-70-1
- FBTOLQFRGURPJH-UHFFFAOYSA-N
- DS-021988
- DTXSID50542243
- 1-Phenyl-carbazol
- DTXCID50493029
- 104636-53-5
- 1-Phenyl-9h-carbazole
- Inchi： 1S/C18H13N/c1-2-7-13(8-3-1)14-10-6-11-16-15-9-4-5-12-17(15)19-18(14)16/h1-12,19H
- InChI Key： FBTOLQFRGURPJH-UHFFFAOYSA-N
- SMILES： N1([H])C2=C([H])C([H])=C([H])C([H])=C2C2C([H])=C([H])C([H])=C(C3C([H])=C([H])C([H])=C([H])C=3[H])C1=2

Computed Properties

Exact Mass: 243.104799g/mol
Monoisotopic Mass: 243.104799g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 0
Heavy Atom Count: 19
Rotatable Bond Count: 1
Complexity: 307
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Topological Polar Surface Area: 15.8
Molecular Weight: 243.3g/mol
XLogP3: 5

1-Phenyl-9h-carbazole Production Method

Production Method 1

877764-42-6

104636-53-5

87666-57-7

Reaction Conditions

1.1 Catalysts: 2497564-99-3 Solvents: Toluene-d8 ; 24 h, 110 °C

Reference

Catalytic C(sp2)-H Amination Reactions Using Dinickel Imides

Powers, Ian G.; et al, Organometallics, 2020, 39(21), 3794-3801

1-Phenyl-9h-carbazole Raw materials

1,1':3',1''-TERPHENYL, 2'-AZIDO-

1-Phenyl-9h-carbazole Preparation Products

1-Phenyl-9h-carbazole Suppliers

Tiancheng Chemical (Jiangsu) Co., Ltd

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(CAS:104636-53-5)1-苯基咔唑

Order Number:LE27029254

Stock Status:in Stock

Quantity:25KG,200KG,1000KG

Purity:99%

Pricing Information Last Updated:Friday, 20 June 2025 13:01

Price ($):discuss personally

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Related Categories

Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Carbazoles

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