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373-53-5

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373-53-5 Usage

Uses

Fluoroiodomethane is an synthetic precursor for the fluoromethylation of radiopharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 373-53-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 373-53:
(5*3)+(4*7)+(3*3)+(2*5)+(1*3)=65
65 % 10 = 5
So 373-53-5 is a valid CAS Registry Number.
InChI:InChI=1/CH2FI/c2-1-3/h1H2

373-53-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name fluoro(iodo)methane

1.2 Other means of identification

Product number -
Other names Fluoromethyl iodide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:373-53-5 SDS

373-53-5Relevant articles and documents

[18F]FMDAA1106 and [18F]FEDAA1106: two positron-emitter labeled ligands for peripheral benzodiazepine receptor (PBR).

Zhang, Ming Rong,Maeda, Jun,Furutsuka, Kenji,Yoshida, Yuichiro,Ogawa, Masanao,Suhara, Tetsuya,Suzuki, Kazutoshi

, p. 201 - 204 (2003)

We synthesized and evaluated N-(5-fluoro-2-phenoxyphenyl)-N-(2-[(18)F]fluoromethyl-5-methoxybenzyl)acetamide ([(18)F]-FMDAA1106) and N-(5-fluoro-2-phenoxyphenyl)-N-(2-[(18)F]fluoroethyl-5-methoxybenzyl)acetamide ([(18)F]FEDAA1106) as two potent radioligan

Direct Monofluoromethylthiolation with S-(Fluoromethyl) Benzenesulfonothioate

Zhao, Qunchao,Lu, Long,Shen, Qilong

supporting information, p. 11575 - 11578 (2017/09/11)

An electrophilic shelf-stable monofluoromethylthiolating reagent S-(fluoromethyl) benezenesulfonothioate (1) was developed. In the presence of a copper catalyst, reagent 1 coupled with a variety of aryl boronic acids to give the corresponding monofluoromethylthiolated arenes in high yields. In addition, addition of reagent 1 to alkyl alkenes in the presence of a silver catalyst gave alkyl monofluoromethylthioethers in high yields.

Crystal Structure and Spectroscopic Investigation of Bromofluoro- and Fluoroiodomethane

Feller, Michael,Lux, Karin,Kornath, Andreas

, p. 5357 - 5362 (2016/01/25)

The solid states of bromofluoromethane (BFM) and fluoroiodomethane (FIM) are characterized by X-ray diffraction analysis and by Raman spectroscopy. The single crystals were obtained by crystallization in situ at low temperature. BFM and FIM crystallize in the space group I2/a and Abm2, respectively. The Raman spectra of both compounds were recorded in different aggregation states and at different temperatures. Quantum chemical calculations and the X-ray diffraction data are considered to describe the noncovalent interactions of both compounds in the solid state. These interactions are discussed in the context of the σ-hole concept.

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