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64818-61-7

Cyclohexane, [(1,1-dimethylethyl)sulfinyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64818-61-7 Structure

  • Basic information

    1. Product Name: Cyclohexane, [(1,1-dimethylethyl)sulfinyl]-
    2. Synonyms:
    3. CAS NO:64818-61-7
    4. Molecular Formula: C10H20OS
    5. Molecular Weight: 188.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64818-61-7.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: Cyclohexane, [(1,1-dimethylethyl)sulfinyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexane, [(1,1-dimethylethyl)sulfinyl]-(64818-61-7)
    11. EPA Substance Registry System: Cyclohexane, [(1,1-dimethylethyl)sulfinyl]-(64818-61-7)

  • 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: 64818-61-7(Hazardous Substances Data)

64818-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64818-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,1 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64818-61:
(7*6)+(6*4)+(5*8)+(4*1)+(3*8)+(2*6)+(1*1)=147
147 % 10 = 7
So 64818-61-7 is a valid CAS Registry Number.

64818-61-7Relevant articles and documents

Thermolysis-Induced Two- or Multicomponent Tandem Reactions Involving Isocyanides and Sulfenic-Acid-Generating Sulfoxides: Access to Diverse Sulfur-Containing Functional Scaffolds

Wu, Shengfeng,Lei, Xiaofang,Fan, Erkang,Sun, Zhihua

, p. 522 - 525 (2018)

Direct reaction of isocyanides with some sulfenic-acid-generating sulfoxides led to the effective formation of the corresponding thiocarbamic acid S-esters in good to high yields. A multicomponent reaction involving isocyanide, sulfoxide, and a suitable nucleophile has also been developed, providing ready access to a diverse range of sulfur-containing compounds, including isothioureas, carbonimidothioic acid esters, and carboximidothioic acid esters.

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