Cas no 15310-02-8 (Benzamide,N-(2-iodophenyl)-)
Benzamide, N-(2-iodophenyl)-, is a halogenated aromatic compound featuring an amide functional group linked to an ortho-iodophenyl substituent. This structure imparts unique reactivity, making it valuable as an intermediate in organic synthesis, particularly in cross-coupling reactions and pharmaceutical applications. The iodine atom enhances its utility in metal-catalyzed transformations, such as Suzuki or Ullmann couplings, while the amide group offers potential for further functionalization. Its well-defined crystalline properties facilitate purification and characterization. The compound’s stability under standard conditions ensures consistent performance in research and industrial processes. Its versatility in constructing complex molecules underscores its importance in medicinal chemistry and material science.
Benzamide,N-(2-iodophenyl)- structure
Product Name:Benzamide,N-(2-iodophenyl)-
CAS No:15310-02-8
MF:C13H10INO
MW:323.129075527191
CID:167266
PubChem ID:285529
Update Time:2025-06-07
Benzamide,N-(2-iodophenyl)- Chemical and Physical Properties
Names and Identifiers
-
- Benzamide,N-(2-iodophenyl)-
- 2-iodophenylbenzamide
- AC1LQN6A
- CBMicro_000122
- CTK1B7674
- N-(2-iodo-phenyl)-2-nitro-benzamide
- N-(2-iodophenyl)benzamide
- N-(2-iodophenyl)-benzamide
- N-(2-iodophenyl)benzaminde
- N-benzoyl-2-iodoaniline
- N-benzoyl-o-iodoaniline
- o-benzoylamidophenyl iodide
- Oprea1_630744
- SMSF0005239
- STK051063
- DTXSID20934676
- AG-777/06841026
- 10.14272/JNLAWMGPPJLSMA-UHFFFAOYSA-N
- Z28163914
- F97442
- doi:10.14272/JNLAWMGPPJLSMA-UHFFFAOYSA-N.1
- Benzamide, N-(2'-iodophenyl)-
- 15310-02-8
- N-(2-Iodophenyl)benzamide #
- MFCD00859420
- SCHEMBL6288808
- doi:10.14272/JNLAWMGPPJLSMA-UHFFFAOYSA-N
- NSC142518
- AKOS001061969
- HMS1759L12
- N-(2-Iodophenyl)benzenecarboximidic acid
- NSC-142518
- 10.14272/JNLAWMGPPJLSMA-UHFFFAOYSA-N.1
-
- Inchi: 1S/C13H10INO/c14-11-8-4-5-9-12(11)15-13(16)10-6-2-1-3-7-10/h1-9H,(H,15,16)
- InChI Key: JNLAWMGPPJLSMA-UHFFFAOYSA-N
- SMILES: IC1C=CC=CC=1NC(C1C=CC=CC=1)=O
Computed Properties
- Exact Mass: 322.9803
- Monoisotopic Mass: 322.981
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 16
- Rotatable Bond Count: 2
- Complexity: 238
- 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: 3.2
- Topological Polar Surface Area: 29.1?2
Experimental Properties
- Density: 1.697
- Boiling Point: 308°Cat760mmHg
- Flash Point: 140.1°C
- Refractive Index: 1.701
- PSA: 29.1
- LogP: 3.61650
Benzamide,N-(2-iodophenyl)- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB592179-250mg |
N-(2-Iodophenyl)benzamide; . |
15310-02-8 | 250mg |
€345.50 | 2024-04-19 | ||
| abcr | AB592179-1g |
N-(2-Iodophenyl)benzamide; . |
15310-02-8 | 1g |
€641.10 | 2024-04-19 |
Benzamide,N-(2-iodophenyl)- Related Literature
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1. N-Heterocyclic carbene copper(i) complex-catalyzed synthesis of 2-aryl benzoxazoles and benzothiazolesJulio I. Urzúa,Renato Contreras,Cristian O. Salas,Ricardo A. Tapia RSC Adv. 2016 6 82401
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Jonathan Clayden,Lluís Vallverdú,Madeleine Helliwell Org. Biomol. Chem. 2006 4 2106
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D. J. C. Prasad,G. Sekar Org. Biomol. Chem. 2013 11 1659
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4. Copper-catalysed intramolecular O-arylation: a simple and efficient method for benzoxazole synthesisFengtian Wu,Jie Zhang,Qianbing Wei,Ping Liu,Jianwei Xie,Haojie Jiang,Bin Dai Org. Biomol. Chem. 2014 12 9696
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Chin Hui Kee,Azhar Ariffin,Khalijah Awang,Koichi Takeya,Hiroshi Morita,Salmaan Inayat Hussain,Kok Meng Chan,Pauline J. Wood,Michael D. Threadgill,Chuan Gee Lim,SeikWeng Ng,Jean Frédéric F. Weber,Noel F. Thomas Org. Biomol. Chem. 2010 8 5646
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