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293329-46-1

di-(l)-menthyl (allylsulfanyl)methylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 293329-46-1 Structure

  • Basic information

    1. Product Name: di-(l)-menthyl (allylsulfanyl)methylphosphonate
    2. Synonyms: di-(l)-menthyl (allylsulfanyl)methylphosphonate
    3. CAS NO:293329-46-1
    4. Molecular Formula:
    5. Molecular Weight: 444.659
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 293329-46-1.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: di-(l)-menthyl (allylsulfanyl)methylphosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: di-(l)-menthyl (allylsulfanyl)methylphosphonate(293329-46-1)
    11. EPA Substance Registry System: di-(l)-menthyl (allylsulfanyl)methylphosphonate(293329-46-1)

  • 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: 293329-46-1(Hazardous Substances Data)

293329-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 293329-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,3,2 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 293329-46:
(8*2)+(7*9)+(6*3)+(5*3)+(4*2)+(3*9)+(2*4)+(1*6)=161
161 % 10 = 1
So 293329-46-1 is a valid CAS Registry Number.

293329-46-1Relevant articles and documents

The first asymmetric synthesis of alpha-sulfanylphosphonates.

Marchand,Gulea,Masson,Saquet,Collignon

, p. 3757 - 3759 (2007/10/03)

[reaction: see text] Diastereoselectivity of up to 88% was achieved for the synthesis of an alpha-mercapto gamma-unsaturated phosphonate using the readily available chiral dimenthylphosphonyl ester group and a carbanionic [2,3]-sigmatropic rearrangement.

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