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1-(Fluoromethyl)-3-iodobenzene is an organic compound with the chemical formula C7H6FI. It is a colorless liquid at room temperature and is characterized by the presence of a fluoromethyl group (-CH2F) attached to the benzene ring at the 1-position and an iodine atom at the 3-position. 1-(fluoromethyl)-3-iodobenzene is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is typically handled under controlled conditions to prevent unwanted side reactions. The compound's properties, such as its boiling point, solubility, and reactivity, make it a valuable building block in the chemical industry for the creation of more complex molecules.

456-45-1

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456-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 456-45-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 456-45:
(5*4)+(4*5)+(3*6)+(2*4)+(1*5)=71
71 % 10 = 1
So 456-45-1 is a valid CAS Registry Number.

456-45-1Relevant academic research and scientific papers

FLUORINATION OF HALOGENO ALCOHOLS WITH 1,1,2,3,3,3-HEXAFLUOROPROPYL DIETHYLAMINE

Watanabe, S.,Fujita, T.,Usui, Y.,Kimura, Y.

, p. 135 - 142 (1986)

Fluorination of halogeno alcohols with 1,1,2,3,3,3-hexafluoropropyl diethylamine (PPDA) was investigated. 2-Bromo-1-fluorobutane was obtained from the reaction of PPDA and 2-bromo-1-butanol (yield 50percent).Similar results were obtained from other alipha

Halogenation through Deoxygenation of Alcohols and Aldehydes

Chen, Jia,Lin, Jin-Hong,Xiao, Ji-Chang

supporting information, p. 3061 - 3064 (2018/05/28)

An efficient reagent system, Ph3P/XCH2CH2X (X = Cl, Br, or I), was very effective for the deoxygenative halogenation (including fluorination) of alcohols (including tertiary alcohols) and aldehydes. The easily available 1,2-dihaloethanes were used as key reagents and halogen sources. The use of (EtO)3P instead of Ph3P could also realize deoxy-halogenation, allowing for a convenient purification process, as the byproduct (EtO)3Pa?O could be removed by aqueous washing. The mild reaction conditions, wide substrate scope, and wide availability of 1,2-dihaloethanes make this protocol attractive for the synthesis of halogenated compounds.

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