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115878-53-0

3-Benzenesulfinyl-3-chloro-1-phenyl-7-phenylsulfanyl-heptan-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115878-53-0 Structure

  • Basic information

    1. Product Name: 3-Benzenesulfinyl-3-chloro-1-phenyl-7-phenylsulfanyl-heptan-4-ol
    2. Synonyms:
    3. CAS NO:115878-53-0
    4. Molecular Formula:
    5. Molecular Weight: 459.073
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115878-53-0.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: 3-Benzenesulfinyl-3-chloro-1-phenyl-7-phenylsulfanyl-heptan-4-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Benzenesulfinyl-3-chloro-1-phenyl-7-phenylsulfanyl-heptan-4-ol(115878-53-0)
    11. EPA Substance Registry System: 3-Benzenesulfinyl-3-chloro-1-phenyl-7-phenylsulfanyl-heptan-4-ol(115878-53-0)

  • 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: 115878-53-0(Hazardous Substances Data)

115878-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115878-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,7 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115878-53:
(8*1)+(7*1)+(6*5)+(5*8)+(4*7)+(3*8)+(2*5)+(1*3)=150
150 % 10 = 0
So 115878-53-0 is a valid CAS Registry Number.

115878-53-0Relevant articles and documents

A Novel and Stereoselective Synthesis of (E)-1-Acylbutadienes from 1-Chloroalkyl Phenyl Sulfoxides and 4-(Phenylthio)butanal through α,β-Epoxy Sulfoxides

Satoh, Tsuyoshi,Motohashi, Shigeyasu,Yamakawa, Koji

, p. 1169 - 1173 (2007/10/02)

The alkylation of 4-(phenylthio)butanal with 1-chloroalkyl phenyl sulfoxides gave chlorohydrins, which were treated with excess thiophenolate in tert-butanol to afford α,δ-bis(phenylthio)ketones in good overall yield.On treatment with m-chloroperbenzoic a

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