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776-70-5

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776-70-5 Usage

Heterocyclic compound

Contains a benzoxazinone ring system

Contains a dimethylamino group

Attached to the benzoxazinone ring system

Potential medicinal and pharmacological properties

Studied for its natural occurrence in certain plants for defense against pathogens and pests

Pharmaceutical intermediate

Being investigated for its potential use in the synthesis of various drugs

Antioxidant properties

Exhibits antioxidant properties, making it potentially useful in the development of antioxidant-based products.

Check Digit Verification of cas no

The CAS Registry Mumber 776-70-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 776-70:
(5*7)+(4*7)+(3*6)+(2*7)+(1*0)=95
95 % 10 = 5
So 776-70-5 is a valid CAS Registry Number.

776-70-5SDS

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 2-(dimethylamino)-1,3-benzoxazin-4-one

1.2 Other means of identification

Product number -
Other names 2-N,N-dimethylamino-1,3-benzoxazin-4-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:776-70-5 SDS

776-70-5Downstream Products

776-70-5Relevant articles and documents

Unexpected ring-expansion of 1,2-benzisoxazol-3-ones

Raw, Steven A.,O'Kearney-Mcmullan, Anne M.,Graham, Mark A.

scheme or table, p. 6775 - 6778 (2012/01/03)

A novel and unexpected ring-expansion reaction of 1,2-benzisoxazol-3-ones is identified. The scope of this reaction is exemplified and the proposed mechanism is also implicated in another degradation process. This reaction also represents a new method for accessing the 4H-1,3-benzoxazin-4-one skeleton.

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