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2-chloro-5-methyl-2-trimethylsilylmethylhexyl phenyl sulphide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77412-07-8 Structure
  • Basic information

    1. Product Name: 2-chloro-5-methyl-2-trimethylsilylmethylhexyl phenyl sulphide
    2. Synonyms:
    3. CAS NO:77412-07-8
    4. Molecular Formula:
    5. Molecular Weight: 329.022
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77412-07-8.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-chloro-5-methyl-2-trimethylsilylmethylhexyl phenyl sulphide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-5-methyl-2-trimethylsilylmethylhexyl phenyl sulphide(77412-07-8)
    11. EPA Substance Registry System: 2-chloro-5-methyl-2-trimethylsilylmethylhexyl phenyl sulphide(77412-07-8)
  • 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: 77412-07-8(Hazardous Substances Data)

77412-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77412-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,1 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77412-07:
(7*7)+(6*7)+(5*4)+(4*1)+(3*2)+(2*0)+(1*7)=128
128 % 10 = 8
So 77412-07-8 is a valid CAS Registry Number.

77412-07-8Downstream Products

77412-07-8Relevant articles and documents

The Formation of Allyl Sulphides by Phenylthio-migration: Control by Silicon

Fleming, Ian,Paterson, Ian,Pearce, Andrew

, p. 256 - 262 (2007/10/02)

When γ-silyl-β-phenylthio-alcohols are treated with acid, the strategically placed silyl group encourages the rearrangement of the phenylthio-group, both from a secondary migration origin to a secondary migration terminus, and from a secondary migration origin to a tertiary migration terminus (4)->(6).Geraniol/nerol (12) and linalool (14) have been synthesised from a common intermediate (11) using this type of reaction.Phenylthio-migration from a tertiary migration origin (17)->(3) can be controlled to a limited extent by a suitably placed silyl group, but it is easier to achieve direct β-elimination of the silyl and phenylthio-groups (17)->(18).

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