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862457-93-0

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862457-93-0 Usage

Physical state

Colorless liquid

Odor

Pungent

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals, key building block for specialty chemicals

Synonyms

4-Phenyl-2-bromo-1,1-difluorobutan-1-one

Hazardous nature

Potential health and environmental risks

Sensitivity

May be sensitive to light and air

Safety measures

Appropriate safety measures should be in place for handling

Check Digit Verification of cas no

The CAS Registry Mumber 862457-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,4,5 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 862457-93:
(8*8)+(7*6)+(6*2)+(5*4)+(4*5)+(3*7)+(2*9)+(1*3)=200
200 % 10 = 0
So 862457-93-0 is a valid CAS Registry Number.

862457-93-0Downstream Products

862457-93-0Relevant articles and documents

Base-catalysed 18F-labelling of trifluoromethyl ketones. Application to the synthesis of 18F-labelled neutrophil elastase inhibitors

Meyer, Denise N.,Cortés González, Miguel A.,Jiang, Xingguo,Johansson-Holm, Linus,Pourghasemi Lati, Monireh,Elgland, Mathias,Nordeman, Patrik,Antoni, Gunnar,Szabó, Kálmán J.

supporting information, p. 8476 - 8479 (2021/09/02)

A new method for the fluorine-18 labelling of trifluoromethyl ketones has been developed. This method is based on the conversion of a-COCF3 functional group to a difluoro enol silyl ether followed by halogenation and fluorine-18 labelling. The utility of this new method was demonstrated by the synthesis of fluorine-18 labelled neutrophil elastase inhibitors, which are potentially useful for detection of inflammatory disorders.

Stereocontrolled synthesis of β-difluoromethylated materials

Nihei, Takashi,Iwai, Noritaka,Matsuda, Tomoko,Kitazume, Tomoya

, p. 5912 - 5915 (2007/10/03)

Investigation of synthetic routes for regio- and stereocontrolled fluorinated materials with a difluoromethyl group, using ethyl bromodifluoroacetate as a starting material, is described. In particular, (E)-difluoromethylated trisubstituted olefins were p

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