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2'-Iodoacetophenone

2'-Iodoacetophenone Structure
CAS No.
2142-70-3
Chemical Name:
2'-Iodoacetophenone
Synonyms
1-(2-Iodophenyl)ethan-1-one;2-IODOACETOPHENONE;1-(2-iodophenyl)ethanone;2-iodophenone;O-IODOACETOPHENONE;2'-IODOACETOPHENONE;2'-Iodoacetophenone;2'-Iodoacetophenone>2''-IODOACETOPHENONE 97%;2'-IODOACETOPHENONE, 99+%
CBNumber:
CB7291551
Molecular Formula:
C8H7IO
Molecular Weight:
246.05
MOL File:
2142-70-3.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

2'-Iodoacetophenone Properties

Boiling point 139-140°C 12mm
Density 1.72 g/mL at 25 °C(lit.)
refractive index n20/D 1.618(lit.)
Flash point 218 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Liquid
Specific Gravity 1.720
color Clear yellow
Sensitive Light Sensitive
BRN 2325078
CAS DataBase Reference 2142-70-3(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P280a-P305+P351+P338-P321-P332+P313-P337+P313-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  C
Risk Statements  36/38
Safety Statements  26-36-24/25
WGK Germany  3
HazardClass  IRRITANT
HS Code  29147000
NFPA 704
1
2 1

2'-Iodoacetophenone price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 540676 2′-Iodoacetophenone 97% 2142-70-3 1G ₹2413.98 2022-06-14 Buy
ALFA India ALF-B25345-06 2'-Iodoacetophenone, 98+% 2142-70-3 5g ₹6076 2022-05-26 Buy
ALFA India ALF-B25345-03 2'-Iodoacetophenone, 98+% 2142-70-3 1g ₹2386 2022-05-26 Buy
TCI Chemicals (India) I0689 2'-Iodoacetophenone min. 98.0 % 2142-70-3 1G ₹2500 2022-05-26 Buy
TCI Chemicals (India) I0689 2'-Iodoacetophenone min. 98.0 % 2142-70-3 5G ₹5300 2022-05-26 Buy
Product number Packaging Price Buy
540676 1G ₹2413.98 Buy
ALF-B25345-06 5g ₹6076 Buy
ALF-B25345-03 1g ₹2386 Buy
I0689 1G ₹2500 Buy
I0689 5G ₹5300 Buy

2'-Iodoacetophenone Chemical Properties,Uses,Production

Chemical Properties

Clear yellow liquid

Uses

2′-Iodoacetophenone (2-Iodoacetophenone) may be used in the synthesis of:
indene derivatives
di-(o-acetylphenyl)acetylene
indenol derivative

Preparation

2'-Iodoacetophenone can be synthesized by diazotization of 2-acetylaniline.
To a solution of p-TsOH (22.80 g, 120 mmol) in CH3CN (160 mL) was added an aromatic amine (40 mmol). The resulting amine salt suspension was cooled to 0-5°C. A solution of NaNO2 (5.52 g, 80 mmol) in H2O (12 mL) and KI (16.6 g, 100 mmol) in H2O (12 mL) were added sequentially. The reaction mixture was stirred for 10 minutes, then allowed to warm to ambient temperature and stirred until all the amine was consumed. To the reaction mixture were then added H2O (700 mL), NaHCO3 (1M; until pH=9-10) and Na2S2O3 (2M, 80 mL). The reaction mixture was extracted with EtOAc and purified by column chromatography (hexanes:EtOAc, 9:1 v/v) to give 2'-iodoacetophenone:yellow oil in 94% yield.

Reactions

2'-Iodoacetophenone is a bioactive molecule that reacts with boronic acids to form aryl boronic acid derivatives. This reaction can be carried out in chlorobenzene or dihedral solvents, and it is scalable and applicable to a variety of boronic acids. The product of this reaction is an organocatalyst for the synthesis of bioactive molecules. 2'-Iodoacetophenone also reacts with dipole-containing additives to form dichlorodiphenyldichloroethane, which has been used as a fungicide, insecticide, and herbicide.

General Description

2′-Iodoacetophenone is a halogenated aromatic ketone.

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2'-Iodoacetophenone Spectrum

2'-IODOACETOPHENONE O-IODOACETOPHENONE 2''-IODOACETOPHENONE 97% 2'-Iodoacetophenone, 98+% 2'-IODOACETOPHENONE, 99+% Ethanone, 1-(2-iodophenyl)- 1-(2-nitrophenyl)-N-[4-[(E)-(2-nitrophenyl)methylideneamino]-1-piperazinyl]methanimine 2'-Iodoacetophenone> 1-(2-iodophenyl)ethanone 2-IODOACETOPHENONE 1-(2-Iodophenyl)ethan-1-one 2-iodophenone 2'-Iodoacetophenone 2142-70-3 IC6H4COCH3 Organic Building Blocks Ketones Building Blocks Carbonyl Compounds C7 to C8 Aromatic Acetophenones & Derivatives (substituted) Adehydes, Acetals & Ketones Iodine Compounds C7 to C8 Carbonyl Compounds Ketones