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(Iodomethyl)oxirane, also known as 1-iodo-2-methyl-oxirane, is a colorless liquid chemical compound with the molecular formula C3H5IO. It has a molecular weight of 200.98 g/mol and is primarily used as a building block in organic synthesis, particularly for the production of pharmaceuticals and agrochemicals. Additionally, it serves as a useful reagent in various chemical reactions such as nucleophilic substitution and cross-coupling reactions. Due to its potential toxicity and flammability, (iodomethyl)oxirane is considered a hazardous substance and should be handled with care.

624-57-7

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624-57-7 Usage

Uses

Used in Pharmaceutical Industry:
(Iodomethyl)oxirane is used as a building block for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the creation of new and innovative drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical industry, (iodomethyl)oxirane is utilized as a key intermediate in the production of various agrochemicals, including pesticides and herbicides. Its reactivity and versatility make it a valuable component in the development of effective and targeted agricultural products.
Used as a Reagent in Chemical Reactions:
(Iodomethyl)oxirane is employed as a reagent in nucleophilic substitution and cross-coupling reactions. Its ability to participate in these reactions contributes to the synthesis of a wide range of organic compounds, further expanding its applications in various chemical and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 624-57-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 624-57:
(5*6)+(4*2)+(3*4)+(2*5)+(1*7)=67
67 % 10 = 7
So 624-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H5IO/c4-1-3-2-5-3/h3H,1-2H2

624-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(iodomethyl)oxirane

1.2 Other means of identification

Product number -
Other names Oxirane,(iodomethyl)

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:624-57-7 SDS

624-57-7Relevant academic research and scientific papers

Facile one-pot transformation of carboxylic acid chlorides into 2-substituted allyl alcohols

Barluenga, Jose,Concellon, Jose M.,Fernandez-Simon, Jose L.,Yus, Miguel

, p. 536 - 537 (2007/10/02)

The reaction of carboxylic acid chlorides (1) with chloromethyl-lithium generated in situ (1:2 molar ratio) in the presence of lithium iodide leads, after hydrolysis, to the corresponding homologated 2-substituted allyl alcohols (2).

Halocyclization of Unsaturated Alcohols and Carboxylic Acids Using Bis(sym-collidine)iodine(I) Perchlorate

Evans, Robert D.,Magee, Joseph W.,Schauble, J. Herman

, p. 862 - 868 (2007/10/02)

Reaction of I(collidine)2(1+) ClO4(1-) with unsaturated alcohols and carboxylic acids in dichloromethane at ambient temperature has afforded three- to seven-membered-ring iodoethers and four- to seven-membered-ring iodolactones, respectively, in moderate

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