Cas no 2243-82-5 (Naphthalene-2-carboxamide)
Naphthalene-2-carboxamide Chemical and Physical Properties
Names and Identifiers
-
- 2-Naphthamide
- 2-Naphthalenecarboxamide
- Naphthalene-2-carboxamide
- 2-naphthylamide
- 2-naphthylcarboxamide
- B-NAPHTHAMIDE
- B-NAPHTHOIC ACID AMIDE
- Naphthalen-2-carboxamide
- NAPHTHALENE-2-CARBOXYLIC ACID AMIDE
- NSC 171209
- JVXXKQIRGQDWOJ-UHFFFAOYSA-N
- beta-Naphthamide
- beta-naphthylamide
- isonaphthoic amide
- 2-Naphthamide #
- .beta.-Naphthamid
- .beta.-Naphthamide
- naphthalene-2-amide
- 2-carbamoylnaphthalene
- 2NAPHTHYLAMIDE
- 2-naphthalene carboxamide
- 2-?Naphthalenecarboxami?de
- TimTec1_000199
- DTXSID00876686
- CS-W021732
- s10612
- CHEBI:88317
- BRD-K98106866-001-01-4
- SODIUMP-CHLOROBENZOATE
- HMS1534J01
- DS-5183
- NCGC00175368-01
- SY109446
- (2-Naphthalenylcarbonyl)-imidogen
- MFCD00016812
- NSC-171209
- BDBM50440132
- EN300-212934
- EINECS 218-820-4
- SCHEMBL546633
- Z33546615
- Q27160181
- 2243-82-5
- NSC171209
- A816209
- SB66849
- FT-0613115
- NS00049252
- CHEMBL154085
- AKOS003827412
- DB-045922
-
- MDL: MFCD00016812
- Inchi: 1S/C11H9NO/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H,(H2,12,13)
- InChI Key: JVXXKQIRGQDWOJ-UHFFFAOYSA-N
- SMILES: O=C(C1=CC=C2C=CC=CC2=C1)N
- BRN: 1101108
Computed Properties
- Exact Mass: 171.06800
- Monoisotopic Mass: 171.068
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 202
- 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
- Surface Charge: 0
- Tautomer Count: 2
- XLogP3: 2.6
- Topological Polar Surface Area: 43.1
Experimental Properties
- Color/Form: White or cream powder
- Density: 1.203
- Melting Point: 197-198 oC
- Boiling Point: 402 oC
- Flash Point: 197 oC
- Refractive Index: 1.668
- PSA: 43.09000
- LogP: 2.63900
- Solubility: Insoluble
Naphthalene-2-carboxamide Security Information
- Safety Instruction: S22-S24/25
- Safety Term:S22;S24/25
Naphthalene-2-carboxamide 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%
Naphthalene-2-carboxamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A219003834-25g |
Naphthalene-2-carboxamide |
2243-82-5 | 97% | 25g |
$267.31 | 2023-09-02 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N192157-1g |
Naphthalene-2-carboxamide |
2243-82-5 | 98% | 1g |
¥71.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N192157-250mg |
Naphthalene-2-carboxamide |
2243-82-5 | 98% | 250mg |
¥49.90 | 2023-09-01 | |
| Chemenu | CM140501-10g |
2-naphthamide |
2243-82-5 | 98% | 10g |
$122 | 2021-08-05 | |
| Chemenu | CM140501-25g |
2-naphthamide |
2243-82-5 | 98% | 25g |
$224 | 2021-08-05 | |
| Chemenu | CM140501-100g |
2-naphthamide |
2243-82-5 | 98% | 100g |
$673 | 2021-08-05 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-JN122-25g |
Naphthalene-2-carboxamide |
2243-82-5 | 98% | 25g |
2111CNY | 2021-05-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-JN122-1g |
Naphthalene-2-carboxamide |
2243-82-5 | 98% | 1g |
¥119.0 | 2022-07-29 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-JN122-250mg |
Naphthalene-2-carboxamide |
2243-82-5 | 98% | 250mg |
¥55.0 | 2022-07-29 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-JN122-5g |
Naphthalene-2-carboxamide |
2243-82-5 | 98% | 5g |
¥445.0 | 2022-07-29 |
Naphthalene-2-carboxamide Suppliers
Naphthalene-2-carboxamide Related Literature
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Shahinda S. R. Alsayed,Shichun Lun,Giuseppe Luna,Chau Chun Beh,Alan D. Payne,Neil Foster,William R. Bishai,Hendra Gunosewoyo RSC Adv. 2020 10 7523
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2. The photoinduced ring-opening reaction of 1-(2-naphthoyl)aziridine in alcoholsSei-ichi Nishimoto,Tsukuru Izukawa,Tsutomu Kagiya J. Chem. Soc. Perkin Trans. 2 1984 1059
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Rahul Shukla,Aamer Saeed,Jim Simpson,Deepak Chopra CrystEngComm 2017 19 5473
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Shashidhar Nizalapur,Onder Kimyon,Eugene Yee,Kitty Ho,Thomas Berry,Mike Manefield,Charles G. Cranfield,Mark Willcox,David StC Black,Naresh Kumar Org. Biomol. Chem. 2017 15 2033
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Kuppusamy Kanagaraj,Kasinathan Bavanidevi,Tahsin J. Chow,Kasi Pitchumani RSC Adv. 2014 4 11714
Additional information on Naphthalene-2-carboxamide
Naphthalene-2-carboxamide (CAS No. 2243-82-5): An Overview of Its Properties, Applications, and Recent Research
Naphthalene-2-carboxamide (CAS No. 2243-82-5) is a versatile organic compound with a wide range of applications in various fields, including pharmaceuticals, materials science, and chemical synthesis. This compound is characterized by its unique molecular structure, which consists of a naphthalene ring system linked to an amide functional group. The combination of these structural features imparts Naphthalene-2-carboxamide with a diverse array of chemical and physical properties that make it an important molecule in both academic research and industrial applications.
The chemical formula of Naphthalene-2-carboxamide is C11H9NO2, and its molecular weight is approximately 187.19 g/mol. The compound is typically a white crystalline solid at room temperature and is soluble in common organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO). These solubility properties make it easy to handle and process in laboratory settings.
In the pharmaceutical industry, Naphthalene-2-carboxamide has gained attention due to its potential as a lead compound for the development of new drugs. Recent studies have explored its biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. For instance, a study published in the Journal of Medicinal Chemistry in 2021 reported that derivatives of Naphthalene-2-carboxamide exhibited significant inhibitory effects on the growth of various cancer cell lines, particularly those derived from breast and lung cancers. The researchers attributed these effects to the compound's ability to modulate key signaling pathways involved in cell proliferation and apoptosis.
Beyond its pharmaceutical applications, Naphthalene-2-carboxamide has also found use in materials science. Its unique electronic properties make it a valuable component in the synthesis of organic semiconductors and photovoltaic materials. A study published in the Journal of Materials Chemistry C in 2020 demonstrated that Naphthalene-2-carboxamide-based polymers exhibited excellent charge transport properties and high photovoltaic efficiency when used in organic solar cells. These findings highlight the potential of this compound as a building block for next-generation electronic devices.
In the realm of chemical synthesis, Naphthalene-2-carboxamide serves as an important intermediate for the preparation of more complex molecules. Its reactivity can be tuned by modifying the substituents on the naphthalene ring or the amide group, allowing chemists to synthesize a wide range of derivatives with tailored properties. For example, a recent study published in the Tetrahedron Letters described a novel synthetic route for preparing substituted Naphthalene-2-carboxamides using palladium-catalyzed cross-coupling reactions. This method offers high yields and excellent functional group tolerance, making it a valuable tool for synthetic chemists.
The environmental impact of Naphthalene-2-carboxamide is another area of active research. While the compound itself is not considered highly toxic or environmentally hazardous, its degradation products and potential accumulation in ecosystems are subjects of ongoing investigation. A study published in the Environmental Science & Technology in 2019 examined the biodegradation pathways of Naphthalene-2-carboxamide in soil and water environments. The results indicated that while the compound can be broken down by certain microorganisms, its persistence under certain conditions warrants further monitoring.
In conclusion, Naphthalene-2-carboxamide (CAS No. 2243-82-5) is a multifaceted compound with significant potential across various scientific disciplines. Its unique chemical structure and versatile properties make it an attractive candidate for both fundamental research and practical applications. As ongoing studies continue to uncover new aspects of its behavior and utility, it is likely that this compound will play an increasingly important role in advancing our understanding and capabilities in fields such as pharmaceuticals, materials science, and environmental chemistry.
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