What is the 4'-Iodoacetophenone?

4'-Iodoacetophenone is brown crystalline powder, while it's Molecular Formula is C8H7IO. brown crystalline powder Synthesis of quinoline-based potential anticancer agents. Substrate for palladium-catalyzed coupling reactions

What is the CAS number for 4'-Iodoacetophenone?

The CAS number of 4'-Iodoacetophenone is 13329-40-3.

What is 4'-Iodoacetophenone (13329-40-3) used for?

4'-Iodoacetophenone is an organic compound with the molecular formula C8H7IO. It is a derivative of acetophenone, featuring an iodine atom attached to the 4' position of the aromatic ring. 4'-Iodoacetophenone is known for its reactivity and is commonly used in various chemical reactions and synthesis processes.InChI:InChI=1/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3

What is the 4'-Iodoacetophenone?

4'-Iodoacetophenone is brown crystalline powder, while it's Molecular Formula is C8H7IO. brown crystalline powder Synthesis of quinoline-based potential anticancer agents. Substrate for palladium-catalyzed coupling reactions

What is the CAS number for 4'-Iodoacetophenone?

The CAS number of 4'-Iodoacetophenone is 13329-40-3.

What is 4'-Iodoacetophenone (13329-40-3) used for?

4'-Iodoacetophenone is an organic compound with the molecular formula C8H7IO. It is a derivative of acetophenone, featuring an iodine atom attached to the 4' position of the aromatic ring. 4'-Iodoacetophenone is known for its reactivity and is commonly used in various chemical reactions and synthesis processes.InChI:InChI=1/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3

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4'-Iodoacetophenone

Name 4'-Iodoacetophenone
CAS 13329-40-3
Purity 99%

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Product Details

Factory Sells Best Quality 4'-Iodoacetophenone 13329-40-3 with GMP standards

Molecular Formula: C8H7IO
Molecular Weight: 246.047
Appearance/Colour: brown crystalline powder
Vapor Pressure: 0.0039mmHg at 25°C
Melting Point: 82-84 °C(lit.)
Refractive Index: 1.603
Boiling Point: 279.9 °C at 760 mmHg
Flash Point: 123.1 °C
PSA： 17.07000
Density: 1.72 g/cm³
LogP: 2.49380

4'-Iodoacetophenone(Cas 13329-40-3) Usage

Synthesis Reference(s)	Journal of the American Chemical Society, 94, p. 5106, 1972 DOI: 10.1021/ja00769a066The Journal of Organic Chemistry, 48, p. 4394, 1983 DOI: 10.1021/jo00171a050
General Description	Pd(0)-catalyzed cross coupling reaction of 4′-iodoacetophenone with siloxane has been reported. Heck-Mizoroki reactions of 4′-iodoacetophenone with styrene catalyzed by Pd nanoparticles in the flow reactor has been reported.

InChI:InChI=1/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3

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13329-40-3 Process route

: 99-90-1
para-bromoacetophenone

: 13329-40-3
4-Iodoacetophenone

: 787-69-9
4,4'-diacetylbiphenyl

Conditions

Conditions	Yield
With tributylphosphine; potassium iodide; nickel dibromide; In N,N,N,N,N,N-hexamethylphosphoric triamide; N,N-dimethyl-formamide; at 50 ℃; for 1.5h;	76 % Chromat. 22 % Chromat.

: 86452-55-3
1-(p-acetophenyl)-3,3-diethyl-1-triazene

: 13329-40-3
4-Iodoacetophenone