chempirical

Naphthol AS

C17H13NO2CAS 92-77-3263.30 g/mol

Open in Covalent MOL file
ONHHO
Phenol

Properties

Molecular formula
C17H13NO2
Molar mass
263.30 g/mol
Exact mass
263.0946 Da
Melting point
296 °C (decomposes)
logP
4.18Crippen estimate
Polar surface area
52.8 Ų
H-bond donors / acceptors
2 / 2
Rotatable bonds
2

Hazards

No GHS classification is on file for this compound. That is not evidence that it is harmless. Search the SDS library

Identifiers

CAS number
92-77-3
SMILES
OC(=Nc1ccccc1)c1cc2ccccc2cc1O
InChIKey
JFGQHAHJWJBOPD-UHFFFAOYSA-N
InChI
InChI=1S/C17H13NO2/c19-16-11-13-7-5-4-6-12(13)10-15(16)17(20)18-14-8-2-1-3-9-14/h1-11,19H,(H,18,20)

Weigh it out

Type any one amount. The others follow from the molar mass.

Names and synonyms

73 names · show all
  • 2-Naphthalenecarboxamide, 3-hydroxy-N-phenyl-
  • 2-Naphthanilide, 3-hydroxy-
  • 3-Hydroxy-N-phenyl-2-naphthalenecarboxamide
  • C.I. 37505
  • Acco naphthol AS
  • Acna naphthol C
  • Amanil naphthol AS
  • Anthonaphthol AS
  • Azoground AS
  • Azonaphthol A
  • Azotol A
  • Brenthol AS
  • Celcot RF
  • Cibanaphthol RF
  • C.I. Azoic coupling component 2
  • Diathol AS
  • Diathol ASF
  • Dragonthol A
  • Hiltonaphthol AS
  • Kambothol AS
  • Lake developer A
  • Mitsui naphthozol AS
  • Naftolo MM
  • Naphthanilide OL supra
  • Naphtanilide RC
  • Naphthanilide RC supra
  • Naphthazol A
  • Naphthoide AS
  • Naphthoide AS no. 100
  • Naphthol ACNA C
  • Naphtholate AS
  • Naphthol AS supra
  • Naphtoelan A
  • Naphtol AS
  • Solunaptol A
  • Tulathol AS
  • Ultrazol I-AS
  • Naphthanil AS
  • 3-Hydroxy-2-naphthanilide
  • 3-(N-Phenylcarbamoyl)-2-naphthol
  • 2-Hydroxy-3-naphthanilide
  • 2-Hydroxy-3-naphthoic anilide
  • 2-Hydroxy-3-naphthalenecarboxanilide
  • 2-Hydroxy-3-naphthoic acid anilide
  • Naphtol AS-A
  • 3-Hydroxy-2-naphthalenecarboxanilide
  • 2-Naphthol-3-carboxylic acid N-phenylamide
  • Amarthol AS
  • 3-Hydroxy-N-phenyl-2-naphthamide
  • 2-Hydroxy-N-phenyl-3-naphthalenecarboxamide
  • 3-Hydroxy-2-naphthoic acid anilide
  • Aquafine red E 9
  • 2-Hydroxy-3-(phenylcarbamoyl)naphthalene
  • α-Naphthol AS
  • N-Phenyl-2-hydroxy-3-naphthalenecarboxamide
  • Azoic coupling component 2
  • Kako grounder AS
  • NSC 45173
  • 3-Hydroxyl-2-naphthanilide
  • Anathol AS
  • Dycosthol AS
  • Hebeithol AS
  • Napthol AS
  • Naftol AS
  • Conazoic coupling B
  • Kiwa grounder AS
  • Orange base GC
  • C.I. Azo coupling comp. 2
  • N-Phenyl-3-hydroxy-2-naphthamide
  • 3-Hydroxy-2-naphthoanilide
  • Sefen AS
  • 3-Hydroxy-naphthalene-2-carboxylic acid phenylamide
  • H 0313

Work with Naphthol AS

Predict the NMR spectrum1H and 13C shifts with multiplicities Make a solutionWhat to weigh for any molarity and volume Check drug-likenessLipinski, Veber and lead-likeness Isotope patternExact mass and the mass spectrum pattern

Similar compounds

3-Hydroxy-N-2-naphthalenyl-2-naphthalenecarboxamide135-64-876 % similar 3-Hydroxy-2-naphthoic acid hydrazide5341-58-266 % similar 3-Hydroxy-N-1-naphthalenyl-2-naphthalenecarboxamide132-68-365 % similar Salicylanilide87-17-264 % similar 3-Hydroxy-3'-nitro-2-naphthanilide135-65-963 % similar 3-Hydroxy-N-(2-methylphenyl)-2-naphthalenecarboxamide135-61-562 % similar 5-Chlorosalicylanilide4638-48-661 % similar 3-Hydroxy-N-(2-methoxyphenyl)-2-naphthalenecarboxamide135-62-657 % similar

Tanimoto similarity of circular fingerprints over the whole catalogue. All similar compounds

Same formula

2-(4-Methylphenyl)-4-quinolinecarboxylic acid20389-05-3

Elsewhere

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