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[Bis(trifluoroacetoxy)iodo]benzene

Catalog No. 232130 Name Sigma Aldrich
CAS Number 2712-78-9 Website http://www.sigmaaldrich.com
M. F. C10H5F6IO4 Telephone 1-800-521-8956
M. W. 430.0391892 Fax
Purity 97% Email
Storage Chembase ID: 8596

SYNONYMS

Title
[双(三氟乙酰氧基)碘]苯
IUPAC name
phenyl[(trifluoroacetyl)oxy]-λ3-iodanyl 2,2,2-trifluoroacetate
IUPAC Traditional name
phenyl[(trifluoroacetyl)oxy]-λ3-iodanyl 2,2,2-trifluoroacetate
Synonyms
Iodobenzene I,I-bis(trifluoroacetate)
PIFA
BTI
I,I-双(三氟乙酸)碘苯

DATABASE IDS

CAS Number 2712-78-9
EC Number 220-308-0
MDL Number MFCD00009672
PubChem SID 24853882
Beilstein Number 764767

PROPERTIES

Linear Formula (CF3CO2)2IC6H5
Purity 97%
Melting Point 121-125 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
10, 50 g in glass bottle
Application
Reactant or reagent for:
• Pummerer-like reactions1,2
• Chemoselective deprotection of dimethoxybenzyl ethers3
• Mediating oxidative cycloisomerization4,5
• Tosyloxylation of anilides6
Used for the direct α-hydroxylation of ketones under acidic conditions. Also employed as a p-fluorination reagent of 4-alkylphenols in the presence of HF·pyridine (cat. no. 184225) for synthesis of 4-fluorocyclohexa-2,5-dienones.Reagent for the oxidation of N-acylhydrazones to 1,3,4-oxadiazoles. Promotes the cyclization of styryl amines to N-alkyl or N-aryl indoles.
Description (简体中文)
包装
10, 50 g in glass bottle
Application
Reactant or reagent for:
• Pummerer-like reactions1,2
• Chemoselective deprotection of dimethoxybenzyl ethers3
• Mediating oxidative cycloisomerization4,5
• Tosyloxylation of anilides6
在酸性条件下用于酮的直接 α-羟基化反应。也可作为 4-烷基酚的对氟化试剂,可在吡啶氢氟酸盐(产品目录号184225)存在的条件下合成 4-氟环己-2,5-二烯酮。 用于 N-酰腙经氧化反应生成 1,3,4-噁二唑的试剂。促进苯乙烯胺环化反应生成 N-烷基吲哚或 N-芳基吲哚。

REFERENCES