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4-Acetyl-2-benzoxazolinone is a yellow crystalline chemical compound belonging to the benzoxazolinone class, characterized by its molecular formula C9H7NO3. It serves as a precursor in the biosynthesis of cyclic hydroxamic acids, which are biologically active natural products. This versatile compound has garnered interest for its potential applications in agriculture and biological research due to its herbicidal properties, allelopathic effects, and roles as an insect deterrent and defense compound in plants.

70735-79-4

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70735-79-4 Usage

Uses

Used in Agricultural Industry:
4-Acetyl-2-benzoxazolinone is used as a herbicide for its ability to inhibit the growth of competing plant species, providing a natural alternative to synthetic chemicals in controlling unwanted vegetation.
Used in Biological Research:
4-Acetyl-2-benzoxazolinone is used as a research compound for studying its role in the biosynthesis of cyclic hydroxamic acids, which have potential applications in various biological processes.
Used in Allelopathic Applications:
4-Acetyl-2-benzoxazolinone is used as an allelopathic agent to induce allelopathic effects, helping to suppress the growth of neighboring plants and thus promoting the dominance of the species it is applied to.
Used as an Insect Deterrent:
4-Acetyl-2-benzoxazolinone is used as an insect deterrent, leveraging its natural properties to protect plants from insect damage and infestation.
Used in Plant Defense Mechanisms:
4-Acetyl-2-benzoxazolinone is used as a defense compound in some plant species, contributing to their resistance against pests and diseases by acting as a natural protective agent.

Check Digit Verification of cas no

The CAS Registry Mumber 70735-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,3 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70735-79:
(7*7)+(6*0)+(5*7)+(4*3)+(3*5)+(2*7)+(1*9)=134
134 % 10 = 4
So 70735-79-4 is a valid CAS Registry Number.

70735-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Acetylbenzo[d]oxazol-2(3H)-one

1.2 Other means of identification

Product number -
Other names 4-acetyl-3H-1,3-benzoxazol-2-one

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:70735-79-4 SDS

70735-79-4Downstream Products

70735-79-4Relevant academic research and scientific papers

Synthesis of 4-acetylbenzoxazolin-2(3H)-one reported from Zea mays

Kluge,Sicker

, p. 821 - 822 (2007/10/03)

A three-step alternative synthesis of 4-acetylbenzoxazolin-2(3H)-one (4) is reported. Starting from inexpensive 3-hydroxyacetophenone (1) 3-hydroxy- 2-nitroacetophenone (2) is prepared by nitration followed by catalytic hydrogenation to yield 2-amino-3-hydroxyacetophenone (3) in which a C=O unit is inserted by means of bis(trichloromethyl)carbonate (triphosgene) in the presence of triethylamine to afford 4 in 35% overall yield.

Biomimetic Synthesis of 4-Acetylbenzoxazolin-2(3H)-one Isolated from Zea mays

Escobar, Carlos A.,Kluge, Michael,Sicker, Dieter

, p. 1407 - 1414 (2007/10/03)

4-Acctylbenzoxazolin-2(3H)-one has been prepared biomimetically during attempts to synthesize the hemiacetalic hydroxamic acid 5-acetyl-2,4-dihydroxy-2H-1,4-benzoxazin-3(4H)-one by the immediate degradation of this unstable compound generated as an intermediate. Thus, 4-acetylbenzoxazolin-2(3H)one recently isolated from Zea mays kernels, and similar to other benzoxazolin-2(3H)-ones known from plant sources, is assumed to have originated from the degradation of natural 5-acetyl-2,4-dihydroxy-2H-1,4-benzoxazin-3(4H)-one which in turn could have been enzymatically released by a β-glucosidase from the corresponding 2-β-D-glucoside.

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