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2-(2,2,2-trifluoroethoxy)-6-trifluoromethylbenzenesulfonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1176126-33-2 Structure
  • Basic information

    1. Product Name: 2-(2,2,2-trifluoroethoxy)-6-trifluoromethylbenzenesulfonyl chloride
    2. Synonyms: 2-(2,2,2-trifluoroethoxy)-6-trifluoromethylbenzenesulfonyl chloride
    3. CAS NO:1176126-33-2
    4. Molecular Formula:
    5. Molecular Weight: 342.646
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1176126-33-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(2,2,2-trifluoroethoxy)-6-trifluoromethylbenzenesulfonyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,2,2-trifluoroethoxy)-6-trifluoromethylbenzenesulfonyl chloride(1176126-33-2)
    11. EPA Substance Registry System: 2-(2,2,2-trifluoroethoxy)-6-trifluoromethylbenzenesulfonyl chloride(1176126-33-2)
  • 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: 1176126-33-2(Hazardous Substances Data)

1176126-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1176126-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,6,1,2 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1176126-33:
(9*1)+(8*1)+(7*7)+(6*6)+(5*1)+(4*2)+(3*6)+(2*3)+(1*3)=142
142 % 10 = 2
So 1176126-33-2 is a valid CAS Registry Number.

1176126-33-2Relevant articles and documents

Penoxsulam-Structure-activity relationships of triazolopyrimidine sulfonamides

Johnson, Timothy C.,Martin, Timothy P.,Mann, Richard K.,Pobanz, Mark A.

experimental part, p. 4230 - 4240 (2009/10/02)

The discovery of the sulfonamide herbicides, which inhibit the enzyme acetolactate synthase (ALS), has resulted in many investigations to exploit their herbicidal activity. One area which proved particularly productive was the N-aryltriazolo[1,5-c]pyrimidine sulfonamides, providing three commercial herbicides, cloransulam-methyl, diclosulam and florasulam. Additional structure-activity investigations by reversing the sulfonamide linkage resulted in the discovery of triazolopyrimidine sulfonamides with cereal crop selectivity and high levels of grass and broadleaf weed control. Research efforts to exploit these high levels of weed activity ultimately led to the discovery of penoxsulam, a new herbicide developed for grass, sedge and broadleaf weed control in rice. Synthetic efforts and structure-activity relationships leading to the discovery of penoxsulam will be discussed.

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