Cas no 62782-37-0 (2-(2-Naphthyloxy)propanoyl chloride)
2-(2-Naphthyloxy)propanoyl chloride Chemical and Physical Properties
Names and Identifiers
-
- Propanoyl chloride, 2-(2-naphthalenyloxy)-
- 2-naphthalen-2-yloxypropanoyl chloride
- 2-(naphthalen-2-yloxy)propanoyl chloride
- MFCD11940523
- 2-(2-NAPHTHYLOXY)PROPANOYL CHLORIDE
- 2-[(Naphthalen-2-yl)oxy]propanoyl chloride
- AKOS005173227
- DTXSID60512093
- VS-04676
- SCHEMBL11406778
- 62782-37-0
- 2-(2-Naphthyloxy)propanoyl chloride
-
- MDL: MFCD11940523
- Inchi: 1S/C13H11ClO2/c1-9(13(14)15)16-12-7-6-10-4-2-3-5-11(10)8-12/h2-9H,1H3
- InChI Key: HAAYQLGWWSPJJD-UHFFFAOYSA-N
- SMILES: ClC(C(C)OC1C=CC2C=CC=CC=2C=1)=O
Computed Properties
- Exact Mass: 234.04483
- Monoisotopic Mass: 234.0447573g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 16
- Rotatable Bond Count: 3
- Complexity: 254
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 4.4
- Topological Polar Surface Area: 26.3?2
Experimental Properties
- PSA: 26.3
2-(2-Naphthyloxy)propanoyl chloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB378875-500 mg |
2-(2-Naphthyloxy)propanoyl chloride |
62782-37-0 | 500MG |
€254.60 | 2023-02-20 | ||
| abcr | AB378875-1 g |
2-(2-Naphthyloxy)propanoyl chloride |
62782-37-0 | 1g |
€322.50 | 2023-05-19 | ||
| abcr | AB378875-5 g |
2-(2-Naphthyloxy)propanoyl chloride |
62782-37-0 | 5g |
€907.00 | 2023-05-19 | ||
| TRC | N233615-250mg |
2-(2-Naphthyloxy)propanoyl chloride |
62782-37-0 | 250mg |
$ 275.00 | 2022-06-03 | ||
| TRC | N233615-500mg |
2-(2-Naphthyloxy)propanoyl chloride |
62782-37-0 | 500mg |
$ 450.00 | 2022-06-03 | ||
| TRC | N233615-1000mg |
2-(2-Naphthyloxy)propanoyl chloride |
62782-37-0 | 1g |
$ 720.00 | 2022-06-03 | ||
| abcr | AB378875-500mg |
2-(2-Naphthyloxy)propanoyl chloride; . |
62782-37-0 | 500mg |
€269.00 | 2025-04-17 | ||
| abcr | AB378875-1g |
2-(2-Naphthyloxy)propanoyl chloride; . |
62782-37-0 | 1g |
€317.00 | 2025-04-17 | ||
| abcr | AB378875-5g |
2-(2-Naphthyloxy)propanoyl chloride; . |
62782-37-0 | 5g |
€877.00 | 2025-04-17 | ||
| abcr | AB378875-10g |
2-(2-Naphthyloxy)propanoyl chloride; . |
62782-37-0 | 10g |
€1357.00 | 2025-04-17 |
2-(2-Naphthyloxy)propanoyl chloride Related Literature
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Dan Yang,Yanping Zhou,Xianhong Rui,Jixin Zhu,Ziyang Lu,Eileen Fong,Qingyu Yan RSC Adv., 2013,3, 14960-14962
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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
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Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
Additional information on 2-(2-Naphthyloxy)propanoyl chloride
2-(2-Naphthyloxy)propanoyl Chloride: A Versatile Building Block in Medicinal Chemistry
2-(2-Naphthyloxy)propanoyl chloride is a key organochloride compound with the CAS No. 62782-37-0, widely recognized for its unique chemical structure and potential applications in pharmaceutical research. This molecule belongs to the class of propanoyl chloride derivatives, characterized by a chlorinated carboxylic acid group attached to a three-carbon chain. The 2-naphthyloxy substituent introduces aromatic functionality, enabling diverse chemical modifications and biological interactions. Recent studies have highlighted its role as a functional group precursor in the development of bioactive molecules, particularly in the context of drug delivery systems and targeted therapy.
The chemical structure of 2-(2-Naphthyloxy)propanoyl chloride consists of a propanoyl chloride moiety linked to a 2-naphthyl ring via an oxygen atom. This structural feature allows for the formation of ester linkages or <
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