ChemicalBook >> CAS DataBase List >>4'-Iodoacetophenone

4'-Iodoacetophenone

CAS No.
13329-40-3
Chemical Name:
4'-Iodoacetophenone
Synonyms
4-IODOACETOPHENONE;1-(4-IODOPHENYL)ETHANONE;p-Iodoacetophenone;4'-iodoaetophenone;4'-IODOACETOPHENONE;4-Acetylphenyl iodide;Of iodine acetophenone;4'-Iodoacetophenone>(4-Acetylphenyl) iodide;4'-Iodoacetophenone 98%
CBNumber:
CB3667820
Molecular Formula:
C8H7IO
Molecular Weight:
246.05
MDL Number:
MFCD00045320
MOL File:
13329-40-3.mol
MSDS File:
SDS
Last updated:2023-11-29 18:07:07

4'-Iodoacetophenone Properties

Melting point 82-84 °C(lit.)
Boiling point 142-144 °C(Press: 12 Torr)
Density 1.7411 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Crystalline Powder
color Pale brown to brown
Water Solubility Easily soluble in water.
Sensitive Light Sensitive
BRN 1857412
InChIKey JZJWCDQGIPQBAO-UHFFFAOYSA-N
CAS DataBase Reference 13329-40-3(CAS DataBase Reference)
FDA UNII 979JX4AA6Z
NIST Chemistry Reference 4-Iodoacetophenone(13329-40-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P280a-P304+P340-P405-P501a-P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39-24/25
WGK Germany  3
HazardClass  IRRITANT
HS Code  29147090
NFPA 704
1
2 0

4'-Iodoacetophenone price More Price(47)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 357804 4′-Iodoacetophenone ≥97% 13329-40-3 5g $41.6 2024-03-01 Buy
Sigma-Aldrich 357804 4′-Iodoacetophenone ≥97% 13329-40-3 25g $54.8 2024-03-01 Buy
TCI Chemical I0305 4'-Iodoacetophenone >98.0%(GC) 13329-40-3 5g $21 2024-03-01 Buy
TCI Chemical I0305 4'-Iodoacetophenone >98.0%(GC) 13329-40-3 25g $68 2024-03-01 Buy
Alfa Aesar A16794 4'-Iodoacetophenone, 98% 13329-40-3 5g $29.65 2024-03-01 Buy
Product number Packaging Price Buy
357804 5g $41.6 Buy
357804 25g $54.8 Buy
I0305 5g $21 Buy
I0305 25g $68 Buy
A16794 5g $29.65 Buy

4'-Iodoacetophenone Chemical Properties,Uses,Production

Chemical Properties

Pale brown to brown crystalline powder

Uses

Synthesis of quinoline-based potential anticancer agents. Substrate for palladium-catalyzed coupling reactions

Synthesis Reference(s)

Journal of the American Chemical Society, 94, p. 5106, 1972 DOI: 10.1021/ja00769a066
The 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.

149104-90-5
13329-40-3
Synthesis of 4'-Iodoacetophenone from 4-Acetylphenylboronic acid
Global( 315)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Mojin Biotechnology Co., Ltd
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CONIER CHEM AND PHARMA LIMITED
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View Lastest Price from 4'-Iodoacetophenone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4'-Iodoacetophenone pictures 2023-11-29 4'-Iodoacetophenone
13329-40-3
US $0.00-0.00 / kg 1kg 99%HPLC 50ton/year Nanjing Fred Technology Co., Ltd
4'-Iodoacetophenone pictures 2023-07-28 4'-Iodoacetophenone
13329-40-3
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
4'-Iodoacetophenone pictures 2023-04-18 4'-Iodoacetophenone
13329-40-3
US $0.00-0.00 / KG 1KG 99% 20 mt Hebei Guanlang Biotechnology Co., Ltd.
4'-IODOACETOPHENONE Of iodine acetophenone 1-Acetyl-4-iodo-benzene 4'-IODOACETOPHENONE FOR SYNTHESIS 4'-Iodoacetophenone 98% 4'-Iodoacetophenone, 97+% Ethanone, 1-(4-iodophenyl)- p-Iodoacetophenone (4-Acetylphenyl) iodide 4-Acetylphenyl iodide Methyl(4-iodophenyl) ketone 4'-Iodoacetophenone,98% 4'-Iodoacetophenone> 4'-iodoaetophenone 1-(4-IODOPHENYL)ETHANONE 4-IODOACETOPHENONE 13329-40-3 C8H7IO KETONE Organic Building Blocks Ketones Building Blocks C7 to C8 Carbonyl Compounds Iodine Compounds C7 to C8 Carbonyl Compounds Ketones Aromatic Acetophenones & Derivatives (substituted) API intermediates Adehydes, Acetals & Ketones