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69804-59-7

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69804-59-7 Usage

General Description

2,7-Dihydroxy-2H-1,4-benzoxazin-3(4H)-one is a natural chemical compound found in plants such as maize, wheat, and rye. It belongs to the class of benzoxazinoids, which are known for their defense properties against herbivores and pathogens. 2,7-Dihydroxy-2H-1,4-benzoxazin-3(4H)-one has been studied for its role in plant defense mechanisms, including its ability to inhibit the growth of certain fungi and bacteria. Additionally, it has been investigated for its potential anti-inflammatory and antioxidant properties, with potential applications in the pharmaceutical and agricultural industries.

Check Digit Verification of cas no

The CAS Registry Mumber 69804-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,0 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69804-59:
(7*6)+(6*9)+(5*8)+(4*0)+(3*4)+(2*5)+(1*9)=167
167 % 10 = 7
So 69804-59-7 is a valid CAS Registry Number.

69804-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dihydroxy-4H-1,4-benzoxazin-3-one

1.2 Other means of identification

Product number -
Other names W2723

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:69804-59-7 SDS

69804-59-7Upstream product

69804-59-7Downstream Products

69804-59-7Relevant articles and documents

First syntheses of natural products with the 2,7-dihydroxy-2H-1,4-benzoxazin-3(4H)-one skeleton

Kluge,Hartenstein,Hantschmann,Sicker

, p. 395 - 402 (2007/10/02)

2,7-Dihydroxy-2H-1,4-benzoxazin-3(4H)-one 11 (DHBOA) and 2,4,7-trihydroxy-2H-1,4-benzoxazin-3(4H)-one 14 (TRIBOA) representing aglucones of naturally occurring acetal glucoside type allelo chemicals found in Gramineae have been for the first time synthesized by two pathways both involving selective reductive cyclizations of appropriate 7-benzyloxy-2-nitrophenol derivatives as precursors. TRIBOA 14 and its bioactive naturally occurring 7-methyl ether DIMBOA have been found to undergo a hitherto unknown transformation to the corresponding 2,6-dibromo substituted lactam forms 20 and 21 in the presence of hydrogen bromide in acetic acid, which is of value in a better understanding of the possible mode of bioactivity.

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