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624-57-7

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624-57-7 Usage

General Description

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

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 articles and documents

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).

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