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105679-37-6

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105679-37-6 Usage

Description

6,8-Dichloro-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride is a chemical compound belonging to the oxazine class of organic compounds. It features a benzene ring fused to an oxazine ring, with chlorine atoms at the 6 and 8 positions on the benzene ring, which confer unique properties to the molecule. 6,8-DICHLORO-3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE HYDROCHLORIDE has demonstrated potential pharmacological applications, particularly as an antipsychotic agent, and has shown promise in preclinical research for the treatment of psychiatric disorders. It has also been investigated for its potential insecticidal and herbicidal properties, although further research is required to fully understand its uses and risks.

Uses

Used in Pharmaceutical Industry:
6,8-Dichloro-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride is used as a potential antipsychotic agent for the treatment of psychiatric disorders. Its unique chemical structure and pharmacological properties have shown promise in preclinical research, making it a candidate for further development and investigation in this field.
Used in Pesticide Industry:
6,8-Dichloro-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride has been investigated for its potential insecticidal properties. Its unique chemical structure may offer new approaches to controlling pests and protecting crops, although further research is needed to fully understand its effectiveness and safety in this application.
Used in Herbicide Industry:
In addition to its potential as an insecticide, 6,8-dichloro-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride has also been studied for its potential herbicidal properties. Its unique chemical structure may provide new options for controlling unwanted plant growth in agricultural and horticultural settings, although more research is required to determine its efficacy and safety in this context.

Check Digit Verification of cas no

The CAS Registry Mumber 105679-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,7 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105679-37:
(8*1)+(7*0)+(6*5)+(5*6)+(4*7)+(3*9)+(2*3)+(1*7)=136
136 % 10 = 6
So 105679-37-6 is a valid CAS Registry Number.

105679-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,8-dichloro-3,4-dihydro-2H-1,4-benzoxazine,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:105679-37-6 SDS

105679-37-6Downstream Products

105679-37-6Relevant articles and documents

Design, synthesis, and bioevaluation of substituted phenyl isoxazole analogues as herbicide safeners

Fu, Ying,Gao, Shuang,Gao, Ying-Chao,Guo, Ke-Liang,Li, Juan-Juan,Wang, Zi-Wei,Ye, Fei,Zhao, Li-Xia

, p. 10550 - 10559 (2020/11/05)

Herbicide safeners enhance herbicide detoxification in crops without affecting target weed sensitivity. To enhance crop tolerance to the toxicity-related stress caused by the herbicide acetochlor (ACT), a new class of substituted phenyl isoxazole derivatives was designed by an intermediate derivatization method as herbicide safeners. Microwave-assisted synthesis was used to prepare the phenyl isoxazole analogues, and all of the structures were confirmed via IR, 1H NMR, 13C NMR, and HRMS. Compound I-1 was further characterized by X-ray diffraction analysis. Bioassay results showed that most of the obtained compounds provided varying degrees of safening against ACT-induced injury by increasing the corn growth recovery, glutathione content, and glutathione S-transferase activity. In particular, compound I-20 showed excellent safener activity against ACT toxicity, comparable to that of the commercial safener benoxacor. Gaussian calculations have been performed and the results indicated that the nucleophilic ability of compound I-20 is higher than that of benoxacor, thus the activity is higher than that of benoxacor. These findings demonstrate that phenyl isoxazole derivatives possess great potential for protective management in cornfields.

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