103543-60-8

Basic information

• Product Name: Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)- (9CI)
• Synonyms: Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)- (9CI);(4-chlorophenyl)(1-fluorocyclopropyl)Methanone
• CAS NO: 103543-60-8
• Molecular Formula: C10H8ClFO
• Molecular Weight: 198.6213232
• Product Categories: ACETYLHALIDE
• Mol File: 103543-60-8.mol

Chemical Properties

• Boiling Point: 75 °C(Press: 0.1 Torr)
• Appearance: /
• Density: 1.31±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)- (9CI)(103543-60-8)
• EPA Substance Registry System: Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)- (9CI)(103543-60-8)

Safety Data

• Hazardous Substances Data: 103543-60-8(Hazardous Substances Data)

Usage

Uses

Used in Organic Chemistry:
Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)(9CI) is used as a synthetic intermediate for [various organic reactions] in the field of organic chemistry. Its unique structure allows for versatile chemical transformations, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)(9CI) is used as a building block for the synthesis of biologically active molecules. Its specific structural features enable the development of new compounds with potential therapeutic applications.
Used in Chemical Research:
Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)(9CI) is also utilized in chemical research as a model compound for studying reaction mechanisms and exploring novel synthetic methodologies. Its unique structural elements provide opportunities for understanding and optimizing chemical reactions.
Used in Specialty Chemicals Production:
Methanone, (4-chlorophenyl)(1-fluorocyclopropyl)(9CI) is used as a key component in the production of specialty chemicals, such as agrochemicals, dyes, and other performance chemicals. Its unique properties contribute to the development of innovative and high-performance products in these industries.

Upstream product

• 3760-66-5 2-bromo-4-chloro-1-(4-chlorophenyl)-butan-1-one 
• 865-47-4 potassium tert-butylate 

Relevant articles and documents

Process for the preparation of 1-fluoro-cyclopropane-1-carboxylic acid

A new process for the preparation of 1-fluoro-cyclopropane-1-carboxylic acid of the formula STR1 which process comprises a) reacting in a first step, a 1-fluoro-cyclopropyl phenyl ketone of the formula STR2 in which R represents hydrogen, halogen, methyl, methoxy, phenyl or phenoxy, with an peroxy compound in the presence of a diluent, and b) reacting, in a second step, the resulting 1-fluoro-cyclopropane-1-carboxylate of the formula STR3 in which R has the abovementioned meaning, with a base in the presence of a diluent, and then acidifying the mixture. New 1-fluoro-cyclopropane-1-carboxylates of the above-mentioned formula.

Substituted azolylmethyl-cyclopropyl-carbinol derivatives

Plant growth-regulating and fungicidal compounds of the formula STR1 in which Ar represents optionally substituted aryl or optionally substituted heteroaryl, R1 represents hydrogen, alkyl, alkenyl, alkynyl, trialkylsilyl, optionally substituted phenylalkyl or an acyl radical, R2 represents halogen, cyano, thiocyano, alkylcarbonyloxy, alkylcarbonylthio or the groupings --X--R3 and --NR4 R5, R3 represents alkyl, cycloalkyl, alkenyl, alkynyl, hydroxyalkyl, alkylthioalkyl, carboxyalkyl, alkoxycarbonylalkyl, optionally substituted aryl, optionally substituted aralkyl or the radical of the formula STR2 R4 and R3 independently of one another represent hydrogen or alkyl, or R4 and R5, together with the nitrogen atom to which they are bonded, represent an optionally substituted cycloaliphatic ring which can contain further heteroatoms, X represents oxygen, sulphur, an SO group or an SO2 group, or R2 furthermore represents hydrogen when Ar represents optionally substituted heteroaryl, and Y represents nitrogen or a CH group, or addition products thereof with acids or metal salts. Novel intermediates are also shown.

Use of azolylmethyl-cyclopropylcarbinol derivatives for combating pseudocercosporella herpotrichoides

Combating Pseudocercosporella herpotrichoides by use of an azolylmethyl-cyclopropyl-carbinol derivative of the formula STR1 in which R1 represents fluorine or chlorine and R2 represents fluorine or chlorine.