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88374-07-6

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88374-07-6 Usage

General Description

2-(2,4-Dichlorophenyl)-2-n-butyl oxirane, also known as 2,4'-(2-n-butyl-1,3-epoxypropane)-dichlorobenzene, is an organic compound that consists of a butyl group attached to an oxirane ring and two chlorine atoms attached to a phenyl group. It is commonly used as a pesticide and a fumigant for controlling insects and pests in agricultural settings. It has low solubility in water and is primarily used in its liquid form. However, this chemical has been criticized for its potential environmental and health hazards, as it is a known irritant and can cause harm to aquatic organisms and wildlife. Due to its potential risks, the use and handling of 2-(2,4-Dichlorophenyl)-2-n-butyl oxirane should be carefully regulated and monitored to prevent negative impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 88374-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88374-07:
(7*8)+(6*8)+(5*3)+(4*7)+(3*4)+(2*0)+(1*7)=166
166 % 10 = 6
So 88374-07-6 is a valid CAS Registry Number.

88374-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Butyl-2-(2,4-dichlorophenyl)oxirane

1.2 Other means of identification

Product number -
Other names 2-(2,4-DICHLOROPHENYL)-2-BUTYL-OXIRANE

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:88374-07-6 SDS

88374-07-6Downstream Products

88374-07-6Relevant articles and documents

Efficient use of trimethylsulfonium methylsulfate as a reagent for the epoxidation of carbonyl-containing compounds

Forrester, Julie,Jones, Ray V. H.,Preston, Peter N.,Simpson, Elizabeth S. C.

, p. 3333 - 3335 (1999)

A process for the efficient conversion of trimethylsulfonium methylsulfate into dimethylsulfonium methanide, thence epoxides, has been devised. Thus dimethyl sulfate and dimethyl sulfide are caused to react in the presence of either a mineral acid or an o

Simple, Inexpensive Synthesis of Oxiranes from Carbonyl Compounds. Generation of Sulfonium Ylides from the Ternary System Methanol-Sulfuric Acid-Dimethyl Sulfide

Forrester, Julie,Jones, Ray V. H,Preston, Peter N.,Simpson, Elisabeth S. C.

, p. 1937 - 1938 (2007/10/02)

Reaction conditions are described for the transformation of benzaldehyde and series of ketones into epoxides, in situ, in the ternary system: methanol-sulfuric acid-dimethyl sulfide.

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