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75823-08-4

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75823-08-4 Usage

Chemical structure

Contains an oxadiazole ring and a 2,4-dichlorophenoxy group.

Usage

Commonly used as a herbicide and plant growth regulator.

Herbicidal action

The 2,4-dichlorophenoxy group selectively kills broadleaf weeds while leaving grasses unaffected.

Popularity

A popular ingredient in many commercial herbicide products due to its selective herbicidal action.

Pharmaceutical applications

The oxadiazole ring may have antitumor, antifungal, and antibacterial properties.

Importance

Significant in both the agricultural and pharmaceutical industries for its herbicidal and medicinal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 75823-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,2 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75823-08:
(7*7)+(6*5)+(5*8)+(4*2)+(3*3)+(2*0)+(1*8)=144
144 % 10 = 4
So 75823-08-4 is a valid CAS Registry Number.

75823-08-4SDS

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 5-[(2,4-dichlorophenoxy)methyl]-3H-1,3,4-oxadiazol-2-one

1.2 Other means of identification

Product number -
Other names -

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:75823-08-4 SDS

75823-08-4Relevant articles and documents

Synthesis of Some New 2-Aryloxymethyl-&δ2-1,3,4-oxadiazolin-5-ones and Their Related Compounds as Potential Pesticides

Singh, H.,Yadav, L. D. S.,Bhattacharya, B. K.

, p. 1006 - 1010 (2007/10/02)

2-Aryloxymethyl-δ2-1,3,4-oxadiazolin-5-ones (II) obtained by cyclisation of N-aryloxyacetyl ureas (I) with Br2/NaOH were treated with aryloxyacetyl chloride, and NH4SCN/benzoyl chloride to yield 4-aryloxyacetyl-2-aryloxy methyl-δ2-1,

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