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1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE, also known as CMME, is an organic compound characterized by its molecular formula C10H11ClO3S. It is a yellow crystalline solid that exhibits solubility in organic solvents. 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE is distinguished by the presence of a chlorine atom, a methyl group, and a methanesulfonyl group attached to a phenyl ring, complemented by an ethanone functional group. Its structural composition endows it with reactivity and versatility, making it a valuable entity in the realm of organic synthesis.

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  • 181997-72-8 Structure
  • Basic information

    1. Product Name: 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE
    2. Synonyms: 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE;1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE(WXC07106)
    3. CAS NO:181997-72-8
    4. Molecular Formula: C10H11ClO3S
    5. Molecular Weight: 246.71
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 181997-72-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 410.5°C at 760 mmHg
    3. Flash Point: 202.1°C
    4. Appearance: /
    5. Density: 1.291g/cm3
    6. Vapor Pressure: 5.98E-07mmHg at 25°C
    7. Refractive Index: 1.53
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE(181997-72-8)
    12. EPA Substance Registry System: 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE(181997-72-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 181997-72-8(Hazardous Substances Data)

181997-72-8 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE is used as a building block for the production of various pharmaceuticals. Its unique structure allows it to serve as a key component in the synthesis of a wide array of medicinal compounds, contributing to the development of novel drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE is utilized as an essential component in the creation of different agrochemicals. Its incorporation aids in the development of innovative products designed to enhance agricultural productivity and manage pests and diseases.
Used in Fine Chemicals Production:
1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE also serves as a fundamental building block in the synthesis of other fine chemicals. Its reactivity and structural diversity make it a preferred choice for the production of specialty chemicals used across various industries.
Used as a Key Intermediate in Chemical Synthesis:
Due to its high reactivity and structural versatility, 1-(2-CHLORO-4-METHANESULFONYL-3-METHYL-PHENYL)-ETHANONE is frequently employed as a key intermediate in the synthesis of a variety of chemical compounds. Its ability to participate in numerous chemical reactions makes it an indispensable tool in the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 181997-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,9,9 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 181997-72:
(8*1)+(7*8)+(6*1)+(5*9)+(4*9)+(3*7)+(2*7)+(1*2)=188
188 % 10 = 8
So 181997-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO3S/c1-6-9(15(3,13)14)5-4-8(7(2)12)10(6)11/h4-5H,1-3H3

181997-72-8Relevant articles and documents

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

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Paragraph 0036-0038, (2016/11/24)

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

-

, (2016/11/14)

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

-

, (2008/06/13)

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

-

, (2008/06/13)

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.

Substituted 4-benzoylpyrazoles

-

, (2008/06/13)

PCT No. PCT/EP97/07210 Sec. 371 Date Jun. 23, 1999 Sec. 102(e) Date Jun. 23, 1999 PCT Filed Dec. 19, 1997 PCT Pub. No. WO98/29392 PCT Pub. Date Jul. 9, 1998The invention relates to 4-benzoylpyrazoles of the formula I and their agriculturally useful salts

2-Anylocyclohexanediones having improved herbicidal properties

-

, (2008/06/13)

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

-

, (2008/06/13)

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 pyrazol-4-ylbenzoyl compounds

-

, (2008/06/13)

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

Herbicidally active phenyldiketone compounds

-

, (2008/06/13)

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

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