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123342-93-8

123342-93-8

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  • 2-Chloro-6-[(4,6-dimethoxy-2-pyrimidinyl)thio]benzoic acid

    Cas No: 123342-93-8

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123342-93-8 Usage

General Description

2-Chloro-6-[(4,6-dimethoxy-2-pyrimidinyl)thio]benzoic acid is a chemical compound belonging to the class of organic compounds known as methoxybenzenes. Its molecular structure comprises a benzoic acid group coupled with a 2-pyrimidinyl group bridged by a sulfur atom. The compound also includes two methoxy groups attached to the pyrimidine ring and a chlorine atom attached to the benzene ring. Although its precise applications are not commonly published, compounds of similar structure have been used in various scientific and industrial applications, often serving as intermediates or precursors to other chemical substances. As with all chemicals, it must be handled appropriately to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 123342-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,3,4 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123342-93:
(8*1)+(7*2)+(6*3)+(5*3)+(4*4)+(3*2)+(2*9)+(1*3)=98
98 % 10 = 8
So 123342-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H11ClN2O4S/c1-19-9-6-10(20-2)16-13(15-9)21-8-5-3-4-7(14)11(8)12(17)18/h3-6H,1-2H3,(H,17,18)

123342-93-8 Well-known Company Product Price

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  • Sigma-Aldrich

  • (09163)  Pyrithiobac  analytical standard

  • 123342-93-8

  • 09163-100MG

  • 5,059.08CNY

  • Detail

123342-93-8SDS

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 pyrithiobac

1.2 Other means of identification

Product number -
Other names 2-chloro-6-[(4,6-dimethoxypyrimidin-2-yl)sulfanyl]benzoic acid

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:123342-93-8 SDS

123342-93-8Downstream Products

123342-93-8Relevant articles and documents

Preparation method of herbicide pyrithiobac-sodium

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Paragraph 0014-0021, (2020/10/04)

The invention relates to a preparation method of herbicide pyrithiobac-sodium, and belongs to the field of plant protection. According to the preparation method, 2-chloro-4, 6-dimethoxypyrimidine is used as a raw material to directly react with 2-chloro-6-mercaptobenzoic acid under the action of a solvent, an inorganic alkali and an alkyl sodium sulfinate catalyst to prepare pyrithiobac-sodium; wherein the alkyl sodium sulfinate catalyst is one of sodium trifluoromethanesulfinate, sodium methanesulfinate, sodium benzenesulfinate and sodium p-toluenesulfinate; the solvent is one or more of methylbenzene, chlorobenzene, acetonitrile, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, N-methyl pyrrolidone and 1, 4-dioxane, and the inorganic alkali is one of potassium carbonate, sodium carbonate and cesium carbonate. The preparation of pyrithiobac-sodium is realized by adopting a clean process technology, and the method has the characteristics of high reaction yield, simple process and the like.

Substituted pyridinesulfonamide compounds or their salts, process for preparing the same, and herbicides containing the same

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, (2008/06/13)

A substituted pyridinesulfonamide compound or its salt represented by the following general formula (I): wherein R1 is an unsubstituted or substituted alkyl group; R2 is an unsubstituted or substituted alkyl group, or an unsubstituted or substituted alkoxy group; and X and Y are each independently a member selected from the group consisting of alkyl groups and alkoxy groups, is disclosed. This compound is useful as the effective ingredient of a herbicide showing a wide weed-control spectrum even if used in a small amount.

Pyrimidine compounds, and herbicidal method and compositions

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, (2008/06/13)

A pyrimidine compound having the formula: STR1 wherein X is a halogen atom, or a salt thereof.

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