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Quizalofop-p-tefuryl solution is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

200509-41-7

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200509-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 200509-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,5,0 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 200509-41:
(8*2)+(7*0)+(6*0)+(5*5)+(4*0)+(3*9)+(2*4)+(1*1)=77
77 % 10 = 7
So 200509-41-7 is a valid CAS Registry Number.

200509-41-7 Well-known Company Product Price

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  • Sigma-Aldrich

  • (33942)  Quizalofop-p-tefurylsolution  100 ng/μL in acetonitrile, PESTANAL®, analytical standard

  • 200509-41-7

  • 33942-2ML

  • 766.35CNY

  • Detail

200509-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-tetrahydrofurfuryl R-2-[4-(6-chloroquinoxalin-2-yloxy)phenoxy]propionate

1.2 Other means of identification

Product number -
Other names quizalofop-p-tefuryl

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:200509-41-7 SDS

200509-41-7Downstream Products

200509-41-7Relevant academic research and scientific papers

A method of synthesizing high-quality kuikui standing grain rice polishings ester

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Paragraph 0026; 0027; 0028; 0029, (2017/08/26)

The invention discloses a synthesis method for high-quality quizalofop-P-tefuryl. The synthesis method comprises the following step: carrying out reaction between (R)-2-[4(6-chloro-2-quinoxalinyl)phenoxyl]ethyl propionate and tetrahydrofurfuryl alcohol under the action of catalyst dibutyltin oxide at the temperature of 90-180 DEG C. By using the method disclosed by the invention, the high-quality quizalofop-P-tefuryl with the content of more than 97% and the optical effective body of more than 97% can be directly obtained without complicated post-treatment, and the reaction yield can reach more than 97%.

Preparation method of quizalofop-p-tefuryl

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Paragraph 0052; 0053; 0054; 0055, (2016/11/21)

The invention provides a preparation method of quizalofop-p-tefuryl. The preparation method comprises the following steps: in the presence of a titanate catalyst, reacting ethyl (R)-2-[4-(6-chloroquinoxalinyl-2-oxy)phenoxy]propionate and tetrahydrofurfuryl alcohol in a nonpolar organic solvent, and carrying out low-temperature refrigeration treatment to obtain the quizalofop-p-tefuryl. Compared with the prior art, the reaction system after reaction is subjected to low-temperature refrigeration treatment to remove inorganic impurities in the organic phase, thereby enhancing the content and appearance of the product; and thus, both the optical content and chemical content of the quizalofop-p-tefuryl are enhanced. The whole method has the advantages of simple production technique, lower equipment cost and no harmful effects on the environment, and is suitable for large-scale industrial production.

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