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66670-98-2

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66670-98-2 Usage

Description

2-(4-methoxyphenyl)-1,3-oxazolidine is a heterocyclic organic compound with the molecular formula C10H13NO2. It features a 4-methoxyphenyl group attached to the second carbon atom in the oxazolidine ring, which contains both nitrogen and oxygen atoms. 2-(4-methoxyphenyl)-1,3-oxazolidine is widely recognized for its role as a chiral auxiliary in asymmetric synthesis, particularly in the production of pharmaceuticals and agricultural chemicals. Its unique structure and properties make it a valuable tool for synthesizing complex organic molecules with specific stereochemistry, and it may also have potential applications in materials science and catalysis.

Uses

Used in Pharmaceutical Industry:
2-(4-methoxyphenyl)-1,3-oxazolidine is used as a chiral auxiliary in asymmetric synthesis for the production of pharmaceuticals. Its unique structure aids in creating complex organic molecules with specific stereochemistry, which is crucial for the development of effective and targeted drugs.
Used in Agricultural Chemicals Industry:
Similarly, in the agricultural chemicals industry, 2-(4-methoxyphenyl)-1,3-oxazolidine serves as a chiral auxiliary in asymmetric synthesis. This helps in the production of agrochemicals with precise molecular structures, ensuring their effectiveness and selectivity in pest control and crop protection.
Used in Materials Science:
2-(4-methoxyphenyl)-1,3-oxazolidine may also be utilized in materials science for the development of new materials with specific properties. Its unique structure can contribute to the creation of materials with tailored characteristics for various applications.
Used in Catalysis:
In the field of catalysis, 2-(4-methoxyphenyl)-1,3-oxazolidine has potential applications due to its ability to influence the stereochemistry of reactions. This can be beneficial in developing more efficient and selective catalytic processes for industrial chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 66670-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,7 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66670-98:
(7*6)+(6*6)+(5*6)+(4*7)+(3*0)+(2*9)+(1*8)=162
162 % 10 = 2
So 66670-98-2 is a valid CAS Registry Number.

66670-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [[(2R,3S,4R,5R)-5-(3-carbamoyl-4H-pyridin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-3H-purin-9-yl)oxolan-2-yl]methyl hydrogen phosphate

1.2 Other means of identification

Product number -
Other names 4-methoxybenzylidene bisdimedone

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:66670-98-2 SDS

66670-98-2Relevant articles and documents

Fragment splicing-based design, synthesis and safener activity of novel substituted phenyl oxazole derivatives

Fu, Ying,Zhang, Dong,Kang, Tao,Guo, You-Yuan,Chen, Wen-Geng,Gao, Shuang,Ye, Fei

supporting information, p. 570 - 576 (2019/01/04)

Fragment splicing is a primary strategy in the design and optimization of leading compound toward new skeleton with target bioactivity. Herein a series of novel substituted phenyl oxazole derivatives were designed via fragment analysis and coupling strategy that led to highly potent and bio-selective herbicide safener. The biological tests showed that most of the compounds could enhance the maize growth index, glutathione content and anti-reverse enzyme glutathione S-transferase activity in vivo. The molecular docking model exhibited that the novel compound could compete with chlorsulfuron binding to the herbicide target enzyme, which consequently attained the herbicide detoxification. Especially compound I-f displayed the best activities than commercial safener isoxadifen-ethyl and other compounds. The present work demonstrates that the synthesized compounds could be developed as potential candidates for the discovery of novel herbicide safeners in the future.

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