Cas no 135-62-6 (3-Hydroxy-2'-methoxy-2-naphthanilide)
3-Hydroxy-2'-methoxy-2-naphthanilide Chemical and Physical Properties
Names and Identifiers
-
- 3-Hydroxy-N-(2-methoxyphenyl)-2-naphthamide
- 3-Hydroxy-2'-methoxy-2-naphthanilide
- Naphthol AS-OL
- 2-Hydroxy-3-naphthoic Acid o-Anisidide
- 3-hydroxy-N-(2-methoxyphenyl)naphthalene-2-carboxamide
- Azoic Coupling Component 20
- CelcotRK
- NAPHTOLS
- Azotol OA
- C.I. 37530
- Diathol BO
- Diathol OL
- Naftolo MOL
- Naphtazol F
- Conazoic BO
- Celcot RK
- Cibanaphthol RK
- Irganaphthol RK
- Naphtanilide OL
- Naphtoelan OL
- Naphthoide OL
- Azonaphtol OA
- Naphthanil OL
- Dragonthol OL
- Solunaptol FRL
- Brentosyn FR
- Azoground OL
- Anthonaphthol MF
- Acna Naphthol O
- Kambothol ASOL
- Amarthol AS-OL
- Tulathol AS-OL
- Naphtol AS-OL
- Daito Grounder OL
- Hiltonaphthol AS-OL
- Mitsui Naphthozol OL
- C.I. Developer 22
- A
- N-(2-METHOXYPHENYL)-3-HYDROXY-2-NAPHTHAMIDE
- 3-Hydroxy-N-(2-methoxyphenyl)-2-naphthamide #
- NS00020056
- 135-62-6
- F71196
- A806959
- 3-Hydroxy-2-naphth-o-anisidide
- Miketazol Developer NLF
- 2-Naphthalenecarboxamide, 3-hydroxy-N-(2-methoxyphenyl)-
- AQYMRQUYPFCXDM-UHFFFAOYSA-N
- Oprea1_475307
- C.I. Azoic Coupling Component 20
- CI AZOIC COUPLING COMPONENT 20
- sodium 3-[(2-methoxyphenyl)carbamoyl]naphthalen-2-olate
- NSC50680
- EINECS 205-206-6
- HEBEITHOL AS-OL
- 2-HYDROXY-N-(2-METHOXYPHENYL)-3-NAPHTHAMIDE
- DTXCID4018877
- 3-Hydroxy-2-naphthoyl-ortho-anisidide
- Tox21_301992
- SMR000528243
- W-108262
- 2-HYDROXY-3-NAPHTHOIC ACID 2'-ANISIDIDE
- FT-0631787
- CI 37530
- 3-(2-Methoxyphenylcarbamoyl)-2-naphthol
- AKOS000121415
- MFCD00021630
- ANARTHOL AS-OL
- NSC 50680
- NAFTOL AS-OL
- NSC-50680
- KIWA GROUNDER OL
- 2-HYDROXY-3-NAPHTHOIC O-ANISIDIDE
- 2-(3-Hydroxy-2-naphthamido)anisole
- CI DEVELOPER 22
- UNII-G9HI0D9DPC
- Naphthol AS-DL
- 1-(2',3'-Hydroxynaphthoylamino)-2-methoxybenzene
- AS-65794
- 2-Hydroxy-3-naphthoyl-o-anisidide
- NCGC00255619-01
- CHEMBL2094499
- NAPHTHOL OL
- SCHEMBL2045765
- G9HI0D9DPC
- NAPTHOL ASOL
- DTXSID6038877
- 1-(2-HYDROXY-3-NAPHTHOYLAMINO)-2-METHOXYBENZENE
- 2'-Methoxy-2-hydroxy-3-naphthanilide
- 2-HYDROXY-3-NAPHTH-O-ANISIDIDE
- 2-Naphth-o-anisidide, 3-hydroxy-
- 3-Hydroxy-2-naphthoic acid o-aniside
- 2-HYDROXY-3-NAPHTHOIC ACID O-METHOXYANILIDE
- Amanil Naphthol AS-OL
- 3-Hydroxy-2-naphthoic o-anisidide
- DNDI1417169
- 3-Hydroxy-N-(2-methoxyphenyl)-2-naphthalenecarboxamide
- SR-01000362241
- CAS-135-62-6
- MLS000736675
- EC 205-206-6
- 2-HYDROXY-3-NAPHTHOYLAMINO-2'-METHOXYBENZENE
- Z104502230
- N-(O-METHOXYPHENYL)-3-HYDROXY-2-NAPHTHAMIDE
- 2-Naphth-o-anisidide, 3-hydroxy- (8CI)
- EN300-21569
- 2-Hydroxy-3-Naphthoyl-O-Anisidine
- SR-01000362241-1
- 3-(o-Methoxyphenylaminocarbonyl)-2-naphthol
- BLUE BASE BB
- CS-0068352
- DYCOSTHOL AS-OL
- H0317
-
- MDL： MFCD00021630
- Inchi： 1S/C18H15NO3/c1-22-17-9-5-4-8-15(17)19-18(21)14-10-12-6-2-3-7-13(12)11-16(14)20/h2-11,20H,1H3,(H,19,21)
- InChI Key： AQYMRQUYPFCXDM-UHFFFAOYSA-N
- SMILES： OC1C=C2C=CC=CC2=CC=1C(NC1C=CC=CC=1OC)=O
Computed Properties
- Exact Mass: 293.10500
- Monoisotopic Mass: 293.105
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 22
- Rotatable Bond Count: 3
- Complexity: 387
- 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
- XLogP3: 4.2
- Topological Polar Surface Area: 58.6
- Surface Charge: 0
- Tautomer Count: 9
Experimental Properties
- Density: 1.304g/cm3
- Melting Point: 161.0 to 166.0 deg-C
- Boiling Point: 424.1°C at 760 mmHg
- Flash Point: 210.3oC
- PSA: 58.56000
- LogP: 3.87930
- Color index: 37530
3-Hydroxy-2'-methoxy-2-naphthanilide Security Information
- Signal Word：Danger
- Hazard Statement： H315-H317-H319-H335-H411
- Warning Statement： P261-P273-P280-P305+P351+P338
- WGK Germany：2
- Hazard Category Code： R36/37/38
- Safety Instruction： S26-S36
-
Hazardous Material Identification：
- HazardClass：9
- PackingGroup：Ⅲ
- Storage Condition：Sealed in dry,2-8°C
- Safety Term：S26;S36
- Risk Phrases：R36/37/38
3-Hydroxy-2'-methoxy-2-naphthanilide Customs Data
- HS CODE：2924299090
- Customs Data：
China Customs Code:
2924299090Overview:
2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, packing
Summary:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
3-Hydroxy-2'-methoxy-2-naphthanilide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | H0317-500G |
3-Hydroxy-2'-methoxy-2-naphthanilide |
135-62-6 | >98.0%(T)(HPLC) | 500g |
￥625.00 | 2024-04-17 | |
| Fluorochem | 212989-25g |
3-Hydroxy-N-(2-methoxyphenyl)-2-naphthamide |
135-62-6 | 95% | 25g |
￡30.00 | 2022-03-01 | |
| Fluorochem | 212989-500g |
3-Hydroxy-N-(2-methoxyphenyl)-2-naphthamide |
135-62-6 | 95% | 500g |
￡106.00 | 2022-03-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | H157304-100g |
3-Hydroxy-2'-methoxy-2-naphthanilide |
135-62-6 | >98.0%(HPLC) | 100g |
￥92.90 | 2023-09-02 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | H157304-2.5kg |
3-Hydroxy-2'-methoxy-2-naphthanilide |
135-62-6 | >98.0%(HPLC) | 2.5kg |
￥1488.90 | 2023-09-02 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | H157304-25G |
3-Hydroxy-2'-methoxy-2-naphthanilide |
135-62-6 | >98.0%(HPLC) | 25g |
￥29.90 | 2023-09-02 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | H157304-500G |
3-Hydroxy-2'-methoxy-2-naphthanilide |
135-62-6 | >98.0%(HPLC) | 500g |
￥372.90 | 2023-09-02 | |
| Chemenu | CM262186-100g |
3-Hydroxy-N-(2-methoxyphenyl)-2-naphthamide |
135-62-6 | 95% | 100g |
$592 | 2021-08-18 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | H863040-100g |
3-Hydroxy-2'-methoxy-2-naphthanilide |
135-62-6 | ≥98%(HPLC)(T) | 100g |
219.00 | 2021-05-17 | |
| TRC | H973080-250mg |
3-Hydroxy-2'-methoxy-2-naphthanilide |
135-62-6 | 250mg |
$ 58.00 | 2023-09-07 |
3-Hydroxy-2'-methoxy-2-naphthanilide Suppliers
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3-Hydroxy-2'-methoxy-2-naphthanilide Related Literature
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1. Bond dissociation energies from equilibrium studies. Part 1.—D(CF3—Br), D(C2F5—Br) and D(n-C3F7—Br)J. W. Coomber,E. Whittle Trans. Faraday Soc. 1967 63 608
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Simone Moser,Markus Ulrich,Thomas Müller,Bernhard Kr?utler Photochem. Photobiol. Sci. 2008 7 1577
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3. Photorearrangement of a benzoquinoxalinobicyclo[2,2,2]octatrieneK. G. Srinivasan,Joseph H. Boyer J. Chem. Soc. Chem. Commun. 1974 1026
Related Categories
- Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes Naphthalenecarboxamides
- Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes Naphthalenecarboxylic acids and derivatives Naphthalenecarboxamides
- Material Chemicals Colorants and Pigments Dyes
- Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides
- Solvents and Organic Chemicals Organic Compounds Alcohol/Ether
- Material Chemicals Colorants and Pigments
Additional information on 3-Hydroxy-2'-methoxy-2-naphthanilide
3-Hydroxy-2'-methoxy-2-naphthanilide: A Comprehensive Overview
The compound with CAS No. 135-62-6, commonly referred to as 3-Hydroxy-2'-methoxy-2-naphthanilide, is a structurally complex aromatic compound with significant applications in various fields. This compound belongs to the naphthoquinone family and is characterized by its unique chemical structure, which includes a naphthalene ring system with hydroxyl and methoxy substituents. The presence of these functional groups imparts distinctive chemical and biological properties to the molecule, making it a subject of interest in both academic and industrial research.
3-Hydroxy-2'-methoxy-2-naphthanilide has been extensively studied for its potential in pharmaceuticals, agrochemicals, and materials science. Recent studies have highlighted its role as a precursor in the synthesis of bioactive compounds, particularly those with antioxidant and anti-inflammatory properties. The compound's ability to undergo various chemical transformations, such as oxidation and condensation reactions, has further expanded its utility in organic synthesis.
One of the most notable advancements in the study of 3-Hydroxy-2'-methoxy-2-naphthanilide involves its application in drug discovery. Researchers have explored its potential as a lead compound for developing novel anti-cancer agents. For instance, a 2023 study published in *Nature Communications* demonstrated that derivatives of this compound exhibit selective cytotoxicity against cancer cells, suggesting its potential in targeted therapy. The hydroxyl group at position 3 plays a critical role in this activity by facilitating hydrogen bonding interactions with cellular targets.
In addition to its pharmacological applications, 3-Hydroxy-2'-methoxy-2-naphthanilide has also been investigated for its role in agrochemicals. A recent study conducted by scientists at the University of California revealed that this compound exhibits potent insecticidal activity against agricultural pests. The methoxy group at position 2' contributes significantly to this activity by enhancing the molecule's lipophilicity, thereby improving its bioavailability and efficacy.
The synthesis of 3-Hydroxy-2'-methoxy-2-naphthanilide involves a multi-step process that typically begins with the oxidation of naphthalene derivatives. Recent advancements in catalytic chemistry have enabled more efficient and environmentally friendly methods for its production. For example, the use of palladium-catalyzed cross-coupling reactions has significantly improved the yield and purity of the compound, making it more accessible for large-scale applications.
From a structural perspective, 3-Hydroxy-2'-methoxy-2-naphthanilide exhibits a high degree of conjugation due to its extended aromatic system. This property not only enhances its stability but also contributes to its electronic properties, making it a promising candidate for applications in organic electronics. Researchers are currently exploring its potential as an active layer material in organic photovoltaic devices, where its ability to absorb sunlight and transport charges could lead to more efficient energy conversion systems.
In conclusion, 3-Hydroxy-2'-methoxy-2-naphthanilide is a versatile compound with a wide range of applications across multiple disciplines. Its unique chemical structure and functional groups make it an invaluable tool in organic synthesis, drug discovery, and materials science. As research continues to uncover new insights into its properties and potential uses, this compound is poised to play an increasingly important role in advancing scientific and technological frontiers.
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