CAS 135-61-5
:3-Hydroxy-N-(2-methylphenyl)-2-naphthalenecarboxamide
Description:
3-Hydroxy-N-(2-methylphenyl)-2-naphthalenecarboxamide, also known by its CAS number 135-61-5, is an organic compound characterized by its complex structure, which includes a naphthalene ring system and an amide functional group. This compound typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its hydrophobic nature due to the aromatic rings. The presence of the hydroxyl group contributes to its potential for hydrogen bonding, which can influence its solubility and reactivity. It is often studied for its biological activity, particularly in the context of medicinal chemistry, where it may exhibit properties such as anti-inflammatory or analgesic effects. The compound's molecular structure allows for various interactions with biological targets, making it of interest in pharmacological research. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C18H15NO2
InChI:InChI=1S/C18H15NO2/c1-12-6-2-5-9-16(12)19-18(21)15-10-13-7-3-4-8-14(13)11-17(15)20/h2-11,20H,1H3,(H,19,21)
InChI key:InChIKey=FBLAHUMENIHUGG-UHFFFAOYSA-N
SMILES:C(NC1=C(C)C=CC=C1)(=O)C2=CC3=C(C=C2O)C=CC=C3
Synonyms:- 1-(2-Hydroxy-3-naphthoylamino)-2-methylbenzene
- 2-Hydroxy-3-Naphthoyl-O-Toluidine
- 2-Hydroxy-3-naphtho-o-toluidide
- 2-Hydroxy-3-naphthoic acid o-toluidide
- 2-Hydroxy-3-naphthoic o-toluidide
- 2-Hydroxy-N-(2-methylphenyl)-3-naphthamide
- 2-Hydroxynaphthalene-3-carbonyl-2′-methylanilide
- 2-Naphthalenecarboxamide, 3-hydroxy-N-(2-methylphenyl)-
- 2-Naphtho-o-toluidide, 3-hydroxy-
- 3-Hydroxy-2-Methyl-2-Naphthanilide
- 3-Hydroxy-2-naphth-o-toluidide
- 3-Hydroxy-2-naphtho-o-toluidide
- 3-Hydroxy-N-(2-methylphenyl)-2-naphthalenecarboxamide
- 3-Hydroxy-N-(o-tolyl)-2-naphthamide
- 3-Hydroxynaphthalene-2-carboxy-o-toluidide
- 3-hydroxy-N-(2-methylphenyl)naphthalene-2-carboxamide
- Acco Naf-Sol AS-D
- Acco Naphthol AS-D
- Acna Naphthol E
- Amanil Naphthol AS-D
- Amarthol AS-D
- Anarthol AS-D
- Anthonaphthol AS-D
- Azobase Red OT
- Azoground D
- Azoic coupling component 18
- Azonaphtol OT
- Azotol OT
- Brenthol OT
- Brentosyn OTN
- Celcot RTO
- Cibanaphthol RTO
- Conazoic AM
- Daito Grounder D
- Dianix Developer ND
- Diathol D
- Dragonthol D
- Dycosthol AS-D
- Hebeithol AS-D
- Hiltonaphthol AS-D
- Kiwa Grounder D
- Miketazol Developer NDF
- Mitsui Naphthozol D
- N-(2-Methylphenyl)-3-hydroxynaphthalene-2-carboxamide
- N-(o-Tolyl)-3-hydroxy-2-naphthamide
- NSC 37188
- Naftol AS-D
- Naftolo MD
- Naphtanilide D
- Naphtanilide D Supra
- Naphtazol D
- Naphthanil AS-D
- Naphthoide AD
- Naphthol AS-D Supra
- Naphthol ASBT
- Naphtoelan D
- Naphtol AS-D
- Naphtol AS-D Supra
- Napthol AD
- Napthol ASD
- Solunaptol OT
- Tulathol AS-D
- Ultrazol D
- naphthol as-D type iii repurified
- C.I. Developer 21
- C.I. Azoic Coupling Component 18
- C.I. 37520
- See more synonyms
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Found 4 products.
3-Hydroxy-2'-methyl-2-naphthanilide
CAS:Formula:C18H15NO2Purity:>97.0%(HPLC)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:277.323-Hydroxy-n-o-tolylnaphthalene-2-carboxamide
CAS:<p>3-Hydroxy-n-o-tolylnaphthalene-2-carboxamide</p>Purity:98%Molecular weight:277.32g/molNaphthol AS-D
CAS:<p>Naphthol AS-D is a diagnostic chemical for phosphatase enzymes and is used to stain cells, tissues, and body fluids for diagnosis. The chemical reacts with the amino groups of proteins in cells and produces a brown color. Naphthol AS-D is not toxic to living cells in concentrations below 5%. It stains basophilic leukemia cells as well as brain cells. This chemical can be used to diagnose cutaneous lesions, such as psoriasis or melanoma, which are difficult to diagnose by standard methods. present in these lesions and produce a brown color.</p>Formula:C18H15NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:277.32 g/mol



