106904-09-0

Basic information

• Product Name: 2-chloro-3-(Methylsulfonyl)benzoic acid
• Synonyms: 2-chloro-3-(Methylsulfonyl)benzoic acid;2-chloro-3-Methyl-4-(Methylsulfonyl)benzoicacid
• CAS NO: 106904-09-0
• Molecular Formula: C₉H₉ClO₄S
• Molecular Weight: 234.65678
• Mol File: 106904-09-0.mol

Chemical Properties

• Boiling Point: 458.9°C at 760 mmHg
• Flash Point: 231.4°C
• Appearance: /
• Density: 1.446g/cm³
• Vapor Pressure: 3.23E-09mmHg at 25°C
• Refractive Index: 1.563
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 2.18±0.28(Predicted)
• CAS DataBase Reference: 2-chloro-3-(Methylsulfonyl)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-3-(Methylsulfonyl)benzoic acid(106904-09-0)
• EPA Substance Registry System: 2-chloro-3-(Methylsulfonyl)benzoic acid(106904-09-0)

Safety Data

• Hazardous Substances Data: 106904-09-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-chloro-3-(Methylsulfonyl)benzoic acid is used as an active pharmaceutical ingredient for its anti-inflammatory and analgesic properties. It is incorporated into various pain-relief medications to reduce pain and swelling by inhibiting the production of certain enzymes involved in the inflammatory response.
Used in Pain Management:
2-chloro-3-(Methylsulfonyl)benzoic acid is used as a pain-relief agent for its ability to alleviate pain and reduce inflammation. It is particularly useful in the treatment of conditions that involve inflammation and pain, such as arthritis and other inflammatory diseases.
Used in Inflammation Treatment:
2-chloro-3-(Methylsulfonyl)benzoic acid is used as an anti-inflammatory agent to treat conditions characterized by inflammation. Its ability to inhibit the production of enzymes involved in the inflammatory response makes it a valuable component in the development of pharmaceuticals for inflammation management.

InChI:InChI=1/C9H9ClO4S/c1-5-7(15(2,13)14)4-3-6(8(5)10)9(11)12/h3-4H,1-2H3,(H,11,12)

Upstream product

• 181997-72-8 2'-chloro-3'-methyl-4'-(methylsulfonyl)acetophenone 
• 181997-71-7 2-chloro-3-methyl-4-methylthio-acetophenone 
• 87-60-5 3-chloro-2-methylbenzenamine 
• 82961-52-2 3-chloro-2-methylphenyl methyl sulfide 
• 95-49-8 2-methylchlorobenzene 
• 82961-57-7 3-Chloro-2-methylphenyl methyl sulphone 

Downstream Products

• 120100-04-1 2-chloro-3-methyl-4-(methylsulfonyl)benzoic acid methyl ester 
• 120100-44-9 methyl 3-bromomethyl-2-chloro-4-methyl-sulfonylbenzoate 
• 120100-77-8 2-chloro-4-(methylsulfonyl)-3-[(2,2,2-trifluoroethoxy)methyl]benzoic acid 
• 263401-21-4 2-chloro-3-(2,2,2-trifluoroethoxy)methyl-4-methanesulfonylbenzoic acid 3-oxo-1-cyclohexenyl ester 
• 335104-84-2 tembotrione 
• 473278-76-1 tefuryltrione 
• 120100-05-2 3-(bromomethyl)-2-chloro-4-methanesulfonylbenzoic acid 

Relevant articles and documents

Process for synthesis of Triketone-based herbicide link sulphur grass alkone

The invention relates to a process for synthesizing triketone herbicide cyclic sulcotrione. The method comprises the following steps: (1) synthesizing 2-chloro-6-methylsulfonyl methylbenzene; (2) synthesizing 2-chloro-3-acetyl-6-methylsulfonyl methylbenzene; (3) synthesizing 2-chloro-3-methyl-4-methylsulfonyl benzoic acid; (4) synthesizing methyl 2-chloro-3-methyl-4-methylsulfonyl benzoate; (5) synthesizing methyl 2-chloro-3-bromomethyl-4-methylsulfonyl benzoate; (6) synthesizing 2-chloro-3-(2,2,2-trifluoroethyoxy)methyl-4-methylsulfonyl benzoic acid; (7) synthesizing 2-chloro-3-(2,2,2-trifluoroethyoxy)methyl-4-methylsulfonyl benzoic acid 3-oxo-1-cyclohexene ester; and (8) synthesizing cyclic sulcotrione. The process disclosed by the invention has the beneficial effects that the reaction steps are reduced, the reaction time is shortened, and the yield of intermediates is improved; the reaction conditions are mild and safe; and the cost is reduced.

Benzoyl compound, composition containing benzoyl compound and application of benzoyl compound

The invention discloses a benzoyl compound, a composition containing the benzoyl compound and application of the benzoyl compound. The formula of the benzoyl compound is as shown in the specification, wherein A, B, X and R are as defined in the specification. The benzoyl compound has high growth inhibition activity on various broad-leaf weeds and gramineae weeds, has no evident phytotoxicity on wheat, has good crop safety, and is few in synthesizing steps, simple in preparation method, low in preparation cost and suitable for large-scale industrial production.

Benzoylcyclohexanediones, process for their preparation and their use as herbicides and plant growth regulators

Benzoylcyclohexanediones of the formula (I), process for their preparation and their use as herbicides and plant growth regulators are described. In this formula (I), R11, R2, R3, R4, R5, R6and R7are various radicals, L is an alkylene chain, and Y and Z are a monoatomic bridge element.

Isoxazolyl- and isoxazolinyl-substituted benzoylcyclohexanediones, process for their preparation and their use as herbicides and plant growth regulators

Isoxazolyl- and isoxazolinyl-substituted benzoylcyclohexanediones, process for their preparation and their use as herbicides and plant growth regulators. Benzoylcyclohexanediones of the formula (I), process for their preparation and their use as herbicides and plant growth regulators are described. In formula (I) R1, R2, R3, R4, R5, R6, R7, Ra, Rb, and Rcare various radicals and Y and Z are a monoatomic bridge element.

2-Anylocyclohexanediones having improved herbicidal properties

Benzoyl derivatives of the formula I STR1 where Z is a 5-membered or 6-membered heterocyclic, saturated or unsaturated radical containing one to three hetero atoms selected from the group consisting of oxygen, sulfur and nitrogen, Q is a cyclohexane-1, 3-

Isoxazolylbenzoyl derivatives

Isoxazol-4-ylbenzoyl derivatives of the formula I STR1 where the substituents have the meanings described in the specification; and agriculturally customary salts thereof.

Herbicidally active phenyldiketone compounds

Herbicidally active phenyldiketone compounds of the formula I STR1 in which the substituents have the following meanings: L and M are hydrogen, C1 -C6 -alkyl, C2 -C6 -alkenyl, C2 -C6 -alkyn

Herbicidally active pyrazol-4-ylbenzoyl compounds

Pyrazol-4-ylbenzoyl compounds of the formula I STR1 where Z is a 5- or 6-membered heterocyclic saturated or unsaturated radical, Q is a pyrazole ring and L and M are as defined in the specification, their use as herbicidal compounds and to processes for p