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ChemicalBook--->CAS DataBase List--->2142-70-3

2142-70-3

2142-70-3 Structure

2142-70-3 Structure
IdentificationMore
[Name]

2'-Iodoacetophenone
[CAS]

2142-70-3
[Synonyms]

2'-IODOACETOPHENONE
2-IODOACETOPHENONE
O-IODOACETOPHENONE
2''-IODOACETOPHENONE 97%
2'-Iodoacetophenone, 98+%
2'-IODOACETOPHENONE, 99+%
[Molecular Formula]

C8H7IO
[MDL Number]

MFCD00094998
[Molecular Weight]

246.05
[MOL File]

2142-70-3.mol
Chemical PropertiesBack Directory
[Appearance]

Clear yellow liquid
[Boiling point ]

139-140°C 12mm
[density ]

1.72 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.618(lit.)
[Fp ]

218 °F
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

Liquid
[color ]

Clear yellow
[Specific Gravity]

1.720
[Sensitive ]

Light Sensitive
[BRN ]

2325078
[CAS DataBase Reference]

2142-70-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

R36/38:Irritating to eyes and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29147000
Raw materials And Preparation ProductsBack Directory
[Preparation Products]

Benzoylacetone-->ETHYL3-METHYL-2-INDOLECARBOXYLATE-->3-PHENYL-1-INDANONE-->3-((tert-butyldimethylsilyl)oxy)-3-cyclohexyl-1-(2-iodophenyl)propan-1-one-->1-(2-((4-fluorophenyl)ethynyl)phenyl)ethanone
Hazard InformationBack Directory
[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 prepared by diazotization of 2-acetylaniline.
[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.
Spectrum DetailBack Directory
[Spectrum Detail]

2'-Iodoacetophenone(2142-70-3)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

[Alfa Aesar]

[Sigma Aldrich]

2142-70-3(sigmaaldrich)
[TCI AMERICA]

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