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Basic Description
| Synonyms | 1-Naphthyl acetate | 830-81-9 | naphthalen-1-yl acetate | 1-Acetoxynaphthalene | alpha-Naphthyl acetate | a-Naphthyl acetate | 1-Naphthol, acetate | Naphthyl acetate | 1-NAPHTHALENOL, ACETATE | Naphthalene, 1-acetoxy- | 1-Naphthalenol, 1-acetate | Acetic acid 1-naphthyl ester | |
|---|---|
| Specifications & Purity | 10mM in DMSO |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
1-Naphthyl acetate is a 1-napthyl ester. Mechanism of photo-Fries rearrangement of 1-naphthyl acetate has been studied using steady state photolysis and laser flash photolysis. product description： 1-Naphthyl acetate is a 1-napthyl ester. Mechanism of photo-Fries rearrangement of 1-naphthyl acetate has been studied using steady state photolysis and laser flash photolysis. Kinetics of photo-Fries rearrangement of 1-napthyl acetate has been studied using steady-state, time-resolved chemically induced dynamic nuclear polarization (CIDNP) and flash photolysis methods. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Benzenoids
- Class Naphthalenes
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Superclass
Benzenoids
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Naphthalenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenes |
| Alternative Parents | Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthalene - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. |
| External Descriptors | a small molecule |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Names and Identifiers
| IUPAC Name | naphthalen-1-yl acetate |
|---|---|
| INCHI | InChI=1S/C12H10O2/c1-9(13)14-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3 |
| InChIKey | VGKONPUVOVVNSU-UHFFFAOYSA-N |
| Smiles | CC(=O)OC1=CC=CC2=CC=CC=C21 |
| Isomeric SMILES | CC(=O)OC1=CC=CC2=CC=CC=C21 |
| WGK Germany | 3 |
| Molecular Weight | 186.21 |
| Beilstein | 2046403 |
| Reaxy-Rn | 2046403 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2046403&ln= |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
| Sensitivity | Moisture sensitive. |
|---|---|
| Flash Point(°F) | >110℃ |
| Flash Point(°C) | >110℃ |
| Boil Point(°C) | 118°C |
| Melt Point(°C) | 49°C |
| Molecular Weight | 186.210 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 186.068 Da |
| Monoisotopic Mass | 186.068 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 212.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Documents & Articles
Fries rearrangement
Categories: Technical articles
Citations of This Product
| 1. Liu Lang, Wang Suji, Zuo Junfeng, Zhang Xiaohe, Peng Xiong, Wang Kang, Chen Maohua. (2023) Characterization and fitness cost of bifenthrin resistance in Rhopalosiphum padi (Hemiptera: Aphididae). JOURNAL OF ECONOMIC ENTOMOLOGY, |
| 2. Xueqing Yang, Xinru Li, Xinzhu Cang, Jianglong Guo, Xiujing Shen, Kongming Wu. (2021) Influence of seasonal migration on the development of the insecticide resistance of oriental armyworm (Mythimna separata) to λ-cyhalothrin. PEST MANAGEMENT SCIENCE, 78 (3): (1194-1205). |
| 3. Yifan Li, Hong Sun, Zhen Tian, Yue Li, Xuan Ye, Ruichi Li, Xinyu Li, Shengli Zheng, Jiyuan Liu, Yalin Zhang. (2021) Identification of key residues of carboxylesterase PxEst-6 involved in pyrethroid metabolism in Plutella xylostella (L.). JOURNAL OF HAZARDOUS MATERIALS, 407 (124612). |
| 4. Zi-Guo Wang, Shan-Shan Jiang, David Mota-Sanchez, Wei Wang, Xin-Ru Li, Yu-Lin Gao, Xu-Peng Lu, Xue-Qing Yang. (2019) Cytochrome P450-Mediated λ-Cyhalothrin-Resistance in a Field Strain of Helicoverpa armigera from Northeast China. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 67 (13): (3546–3553). |
| 5. Li-sha Bai, Cai-xia Zhao, Jing-jing Xu, Chuan Feng, Yong-qiang Li, Yan-ling Dong, Zhi-qing Ma. (2019) Identification and biochemical characterization of carboxylesterase 001G associated with insecticide detoxification in Helicoverpa armigera. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 157 (69). |
| 6. Lu Xu, Jun Zhao, Yang Sun, Dejin Xu, Guangchun Xu, Xiaolong Xu, Yueliang Zhang, Shuijin Huang, Zhaojun Han, Zhongyan Gu. (2018) Constitutive overexpression of cytochrome P450 monooxygenase genes contributes to chlorantraniliprole resistance in Chilo suppressalis (Walker). PEST MANAGEMENT SCIENCE, 75 (3): (718-725). |
| 7. Yunhe Zhao, Shuangyu Xu, Hongbao Lu, Daxia Zhang, Feng Liu, Jin Lin, Chenggang Zhou, Wei Mu. (2017) Effects of the plant volatile trans‑2-hexenal on the dispersal ability, nutrient metabolism and enzymatic activities of Bursaphelenchus xylophilus. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 143 (147). |
| 8. Yongqiang Li, Jianwei Liu, Mei Lu, Zhiqing Ma, Chongling Cai, Yonghong Wang, Xing Zhang. (2016) Bacterial Expression and Kinetic Analysis of Carboxylesterase 001D from Helicoverpa armigera. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 17 (4): (493). |
| 9. Hong-Xue Qi,Hui-Zhen Li,Ping Ma,Jing You. (2015-05-26) Integrated sediment quality assessment through biomarker responses and bioavailability measurements: Application in Tai Lake, China.. Ecotoxicology and environmental safety, 119 (148-154). |
| 10. Xiaodan Yan,Jianjun Wang,Yu Sun,Junge Zhu,Sheng Wu. (2016-10-30) Facilitating the Evolution of Esterase Activity from a Promiscuous Enzyme (Mhg) with Catalytic Functions of Amide Hydrolysis and Carboxylic Acid Perhydrolysis by Engineering the Substrate Entrance Tunnel.. Applied and environmental microbiology, 82 ((22)): (6748-6756). |
| 11. Xingyue Luo, Chun Ji, Xiao Wang, Laping He, Yuangen Wu, Han Tao. (2025) A plant esterase-catalyzed electrochemical sensing strategy for organophosphorus pesticide using 2,6-dichlorophenolindophenol as signal probe and FeSAC-NPC as electrocatalyst. MICROCHEMICAL JOURNAL, 211 (113129). |
| 12. Yongmei Chang, Weihuan Xu, Shan Wang, Mengyao Zhu, Yanan Ru, Zhiheng Xu, Guangyou Chen, Yongqiang Li. (2024) Characterization of Four Carboxylesterases Involved in Detoxification of β-Cypermethrin, λ-Cyhalothrin, and Malathion in Helicoverpa armigera. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 72 (46): (25533-25548). |
| 13. Donglin Xiang, Shuyi Qiu, Laping He, Chun Ji, Jiayu Chen, Yuangen Wu, Han Tao. (2024) Purification, characterization of a plant esterase from red kidney bean and its feasibility for pesticide residue analysis in foods. Food Bioscience, 59 (103944). |
| 14. Shuqi Xing, Wei Xie, Guangli Hu, Chaocheng Luo, Hong Zhu, Laping He, Cuiqin Li, Xiao Wang, Xuefeng Zeng. (2025) The synthesis of cinnamyl acetate and deacetyl-7-aminocephalosporanic acid by a GDSL-type esterase and its substrate specificity analysis. ENZYME AND MICROBIAL TECHNOLOGY, 182 (110532). |
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