25116-37-4

Basic information

• Product Name: 3-IODOBENZOPHENONE
• Synonyms: 3-IODOBENZOPHENONE;(3-IODOPHENYL)PHENYLMETHANONE
• CAS NO: 25116-37-4
• Molecular Formula: C₁₃H₉IO
• Molecular Weight: 308.11
• Mol File: 25116-37-4.mol
• Article Data: 13

Chemical Properties

• Melting Point: 44 °C
• Boiling Point: 379.9°C at 760 mmHg
• Flash Point: 183.6°C
• Appearance: /
• Density: 1.624g/cm³
• Vapor Pressure: 5.67E-06mmHg at 25°C
• Refractive Index: 1.647
• CAS DataBase Reference: 3-IODOBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-IODOBENZOPHENONE(25116-37-4)
• EPA Substance Registry System: 3-IODOBENZOPHENONE(25116-37-4)

Safety Data

• Hazardous Substances Data: 25116-37-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H9IO/c14-12-8-4-7-11(9-12)13(15)10-5-2-1-3-6-10/h1-9H

Upstream product

• 1711-10-0 3-iodobenzoyl chloride 
• 71-43-2 benzene 
• 2835-78-1 3-amino benzophenone 
• 100-58-3 phenylmagnesium bromide 
• 618-51-9 3-Iodobenzoic acid 
• 90434-01-8 3-iodo-N-methylbenzamide 
• 696-41-3 m-iodobenzaldehyde 
• 119-61-9 benzophenone 
• 98-88-4 benzoyl chloride 

Downstream Products

• 92903-39-4 1-benzyl-3-iodobenzene 
• 71953-00-9 (2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)propionic acid tert-butyl ester 
• 381222-40-8 (2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(3'-benzoylphenyl)propionic acid tert-butyl ester 
• 75116-78-8 ethyl α-(3-benzoylphenyl)acrylate 
• 1244029-39-7 C₃₃H₃₄O₅ 
• 1214274-01-7 C₁₃H₉⁽¹⁸⁾FO 
• 81601-93-6 (R)-(-)-2-(3-benzoylphenyl)propionic acid methyl ester 
• 13020-57-0 3-hydroxybenzophenone 
• 22161-81-5 S-ketoprofen 
• 1276111-31-9 (4-(phenylcarbonyl)phenyl)(mesityl)iodonium trifluoromethylsulfonate 
• 2835-78-1 3-amino benzophenone 
• 1169763-38-5 3-monoperfluorooctyl benzophenone 
• 91-01-0 1,1-Diphenylmethanol 
• 84359-23-9 (3-iodophenyl)(phenyl)methanol 

Relevant articles and documents

Chemoselective Synthesis of Aryl Ketones from Amides and Grignard Reagents via C(O)-N Bond Cleavage under Catalyst-Free Conditions

Conversion of a wide range of N-Boc amides to aryl ketones was achieved with Grignard reagents via chemoselective C(O)-N bond cleavage. The reactions proceeded under catalyst-free conditions with different aryl, alkyl, and alkynyl Grignard reagents. α-Ketoamide was successfully converted to aryl diketones, while α,β-unsaturated amide underwent 1,4-addition followed by C(O)-N bond cleavage to provide diaryl propiophenones. N-Boc amides displayed higher reactivity than Weinreb amides with Grignard reagents. A broad substrate scope, excellent yields, and quick conversion are important features of this methodology.

Application of [Hcpy]HSO4 Broensted acidic ionic liquid for the synthesis of aryl iodides from aromatic amines

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Designed synthesis of multi-electrochromic systems bearing diaryl ketone and isophthalates

New multi-electrochromic systems have been developed through the combination of a diaryl ketyl radical system with isophthalate-based electrochromic materials. The location of the isophthalate group in compounds is very critical to obtaining different colors in the multi-electrochromism.