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3,4-Dihydro-2H-1,4-benzoxazine-2-carbonitrile, a heterocyclic organic compound with the molecular formula C9H6N2O, features a benzene ring fused to an oxazine ring and a cyano group. 3,4-DIHYDRO-2H-1,4-BENZOXAZINE-2-CARBONITRILE is recognized for its potential as a building block in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its unique structure and properties also suggest possible applications in materials science and polymer chemistry, with ongoing research into its biological activities and pharmacological properties.

86267-86-9

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86267-86-9 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Dihydro-2H-1,4-benzoxazine-2-carbonitrile is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug molecules. Its structural features allow for the creation of diverse chemical entities with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3,4-Dihydro-2H-1,4-benzoxazine-2-carbonitrile serves as a precursor in the production of agrochemicals, aiding in the design of new compounds with pesticidal or herbicidal properties, thereby enhancing crop protection strategies.
Used in Materials Science:
3,4-Dihydro-2H-1,4-benzoxazine-2-carbonitrile is utilized in materials science for its potential to form new polymers or contribute to the modification of existing materials, improving their performance characteristics for various applications.
Used in Polymer Chemistry:
3,4-DIHYDRO-2H-1,4-BENZOXAZINE-2-CARBONITRILE is employed in polymer chemistry to develop new types of polymers with specific properties, such as enhanced stability, reactivity, or selectivity in chemical processes, by incorporating its unique structural elements into polymer backbones.

Check Digit Verification of cas no

The CAS Registry Mumber 86267-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86267-86:
(7*8)+(6*6)+(5*2)+(4*6)+(3*7)+(2*8)+(1*6)=169
169 % 10 = 9
So 86267-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c10-5-7-6-11-8-3-1-2-4-9(8)12-7/h1-4,7,11H,6H2

86267-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-Dihydro-2H-benzo[b][1,4]oxazine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 3,4-DIHYDRO-2H-1,4-BENZOXAZINE-2-CARBONITRILE

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:86267-86-9 SDS

86267-86-9Relevant academic research and scientific papers

NOVEL BENZYL SULFONAMIDE COMPOUNDS USEFUL AS MOGAT-2 INHIBITORS

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Page/Page column 14-15, (2014/05/24)

The present invention provides compounds of Formula I. Wherein Rl, L, and A are as described herein, or a pharmaceutical salt thereof, processes for preparing the compounds, and methods of treating a condition, such as hypertriglyceridemia, using the comp

Zur Synthese von 3,4-Dihydro-2H-1,4-benzoxazin-2- und 3-carbonitrilen. 11. Mitteilung ueber Studien zur Chemie der 1,4-Oxazine

Bartsch, Herbert,Schwarz, Otto

, p. 45 - 48 (2007/10/02)

Reaction of o-aminophenols 1a, 1b and 1c with alkyl dibromopropionates selectively leads to 2-substituted dihydro-1,4-benzoxazines.This high regioselectivity is explained by initial elimination of hydrogen bromide from the dibromopropionate to form a reac

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