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Benzamide, N-(3-iodophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52807-28-0 Structure
  • Basic information

    1. Product Name: Benzamide, N-(3-iodophenyl)-
    2. Synonyms:
    3. CAS NO:52807-28-0
    4. Molecular Formula: C13H10INO
    5. Molecular Weight: 323.133
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52807-28-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzamide, N-(3-iodophenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, N-(3-iodophenyl)-(52807-28-0)
    11. EPA Substance Registry System: Benzamide, N-(3-iodophenyl)-(52807-28-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 52807-28-0(Hazardous Substances Data)

52807-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52807-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,0 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52807-28:
(7*5)+(6*2)+(5*8)+(4*0)+(3*7)+(2*2)+(1*8)=120
120 % 10 = 0
So 52807-28-0 is a valid CAS Registry Number.

52807-28-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid-(3-iodo-anilide)

1.2 Other means of identification

Product number -
Other names Benzoylderivat von m-Jodanilin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52807-28-0 SDS

52807-28-0Downstream Products

52807-28-0Relevant articles and documents

N-Phenylbenzamide derivatives as alternative oxidase inhibitors: Synthesis, molecular properties, 1H-STD NMR, and QSAR

Barsottini, Mario R. O.,Carazzolle, Marcelo F.,Costa, Paulo C. S.,Evangelista, Joel S.,Miranda, Paulo C. M. L.,Nascimento, Andrey F. Z.,Pereira, Gon?alo A. G.,Pires, Bárbara A.,Rocco, Silvana A.,Sfor?a, Maurício L.,Silva, Jaqueline S.,Vieira, Maria L. L.,Zeri, Ana C. M.

, (2020/02/27)

In the present work, 117 N-phenylbenzamides (NPDs) were prepared and evaluated against recombinant AOX from the fungal pathogen Moniliophthora perniciosa. 1H, 13C NMR, FTIR, and mass spectra provided structural information on NPDs. The library compounds were tested as Alternative Oxidase inhibitors in two different assays using the model yeast Pichia pastoris: cell growth and oxygen consumption assays. The most active compound, 3FH, was further characterized by DRX and 1H-NMR-STD. Single crystal X-ray diffraction showed intra- and intermolecular interactions of 3FH in solid-state and elucidated its 3D structural configuration. 1H-NMR-STD allowed us to derive protein-ligand interactions in a membrane-mimetic system and evidenced an outstanding interaction of 3FH with this enzyme. Results of both biological assays were used as input to Quantitative Structure-Activity Relationship models, which highlighted the more important molecular fragments contributions for protein-ligand interaction.

Palladium/copper tandem catalysis for carbon-carbon triple bond cleavage of diaryl acetylenes

Wang, Zhiwei,Fan, Wenyou,Deng, Guo-Jun,Zhou, Wang

supporting information, p. 5449 - 5452 (2015/09/15)

A method for carbon-carbon triple bond cleavage based on palladium/copper tandem catalysis is developed. In this chemistry, anilines and diaryl acetylenes were converted into benzamides through cascade transformations combining palladium-catalyzed hydroamination of alkyne with copper-catalyzed aerobic oxidative C-C bond cleavage.

Copper-Catalyzed N-Benzoylation of Amines via Aerobic C-C Bond Cleavage

Fan, Wenyou,Yang, Youqing,Lei, Jianhua,Jiang, Qijian,Zhou, Wang

, p. 8782 - 8789 (2015/09/15)

A general copper/air catalytic system for selectively oxidative C-C bond cleavage of 1,2-diarylethan-1-one has been developed, giving aromatic aldehydes and N-benzoylation products of various amines in moderate to excellent yields. This research provides an alternative approach for the N-benzoylation of amine in mild and neutral conditions.

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