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CAS

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1612226-10-4

1-(2,4-dimethylphenyl)-2-((trifluoromethyl)thio)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1612226-10-4 Structure

  • Basic information

    1. Product Name: 1-(2,4-dimethylphenyl)-2-((trifluoromethyl)thio)ethanone
    2. Synonyms: 1-(2,4-dimethylphenyl)-2-((trifluoromethyl)thio)ethanone
    3. CAS NO:1612226-10-4
    4. Molecular Formula:
    5. Molecular Weight: 248.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1612226-10-4.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: 1-(2,4-dimethylphenyl)-2-((trifluoromethyl)thio)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2,4-dimethylphenyl)-2-((trifluoromethyl)thio)ethanone(1612226-10-4)
    11. EPA Substance Registry System: 1-(2,4-dimethylphenyl)-2-((trifluoromethyl)thio)ethanone(1612226-10-4)

  • 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: 1612226-10-4(Hazardous Substances Data)

1612226-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1612226-10-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,2,2,2 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1612226-10:
(9*1)+(8*6)+(7*1)+(6*2)+(5*2)+(4*2)+(3*6)+(2*1)+(1*0)=114
114 % 10 = 4
So 1612226-10-4 is a valid CAS Registry Number.

1612226-10-4Downstream Products

1612226-10-4Relevant articles and documents

Copper-catalyzed synthesis of α-trifluoromethylthio-substituted ketones

Huang, Yangjie,He, Xing,Lin, Xiaoxi,Rong, Mingguang,Weng, Zhiqiang

, p. 3284 - 3287 (2014)

The CF3S-substituted moiety serves as an important structural element in many bioactive molecules. A versatile copper catalyst that allowed for trifluoromethylthiolation of primary and secondary α-bromoketones is described. The reaction with readily available elemental sulfur and CF 3SiMe3 afforded a broad scope and moderate to good yields of α-trifluoromethylthio-substituted ketones. This procedure represents a very operationally simple yet powerful strategy for the synthesis of α-trifluoromethylthio-substituted ketones, a useful and versatile class of synthetic synthons.

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