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7-Methyl-2,4-dihydro-1,4-benzoxazin-3-one, commonly known as DIMBOA, is a naturally occurring compound predominantly found in plants like maize and wheat. It is a member of the benzoxazinoid class, which are recognized for their defensive roles against herbivores and microbes. DIMBOA plays a crucial part in the plant's immune system, being synthesized in response to stress factors such as herbivory and pathogen invasion. Beyond its role in plant defense, DIMBOA has garnered interest for its potential applications in agriculture and medicine, including its use as a natural pesticide and for its antioxidant and anti-inflammatory properties. It is also being studied for its possible benefits to human health as a dietary antioxidant.

39522-25-3

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39522-25-3 Usage

Uses

Used in Agricultural Applications:
7-Methyl-2,4-dihydro-1,4-benzoxazin-3-one is used as a natural pesticide for its anti-herbivore and antimicrobial properties, helping to protect crops from insects and pathogens without the need for synthetic chemicals.
Used in Medicinal Applications:
7-Methyl-2,4-dihydro-1,4-benzoxazin-3-one is used as an antioxidant and anti-inflammatory agent due to its potential health benefits, which include reducing oxidative stress and inflammation in the body.
Used in Human Health Research:
7-Methyl-2,4-dihydro-1,4-benzoxazin-3-one is being investigated for its role as a dietary antioxidant, which may contribute to overall health and well-being by combating free radicals and supporting the immune system.

Check Digit Verification of cas no

The CAS Registry Mumber 39522-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,2 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39522-25:
(7*3)+(6*9)+(5*5)+(4*2)+(3*2)+(2*2)+(1*5)=123
123 % 10 = 3
So 39522-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO2/c1-6-2-3-7-8(4-6)12-5-9(11)10-7/h2-4H,5H2,1H3,(H,10,11)

39522-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methyl-4H-1,4-benzoxazin-3-one

1.2 Other means of identification

Product number -
Other names 7-methyl-3-oxo-2,3-dihydro-4H-1,4-benzoxazine

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:39522-25-3 SDS

39522-25-3Relevant academic research and scientific papers

Isolation and characterization of 2-alkylaminobenzo[b]furans. Evidence for competing O-arylation in Cu-catalyzed intramolecular amidation

Feng, Gaofeng,Wu, Jinlong,Dai, Wei-Min

, p. 401 - 404 (2008/02/04)

2-Alkylaminobenzo[b]furans were isolated and characterized by X-ray crystal structural analysis, for the first time, from the Cu-catalyzed intramolecular amidation of hindered secondary amides under controlled microwave heating. A mechanism was proposed t

BENZOXAZINE DERIVATIVES AS INHIBITORS OF LEUKOTRIENES

-

, (2008/06/13)

The invention concerns a bicyclic heterocyclic compound of the formula I wherein Q is an optionally substituted 10-membered bicyclic heterocyclic moiety containing 1 or 2 N's and a further O or S heteroatom; A1 is a direct link to X1 or (1-3C)alkylene; X1 is oxy, thio, sulphinyl, sulphonyl or imino; Ar is optionally substituted phenylene or pyridylene; R1 is (1-4C)alkyl, (3-4C)alkenyl or (3-4C)alkynyl; and R2 and R3 together form a group of the formula -A2-X2-A3- which, together with the carbon atom to which A2 and A3 are attached, defines a ring having 5 to 7 ring atoms, wherein each of A2 and A3 is (1-3C)alkylene and X2 is oxy, thio, sulphinyl or sulphonyl; or a pharmaceutically-acceptable salt thereof. The compounds of the invention are inhibitors of the enzyme 5-lipoxygenase

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