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CAS

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1360819-67-5

(Z)-3,3-dimethyl-1-(phenylthio)hexa-1,5-dien-2-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1360819-67-5 Structure

  • Basic information

    1. Product Name: (Z)-3,3-dimethyl-1-(phenylthio)hexa-1,5-dien-2-yl acetate
    2. Synonyms:
    3. CAS NO:1360819-67-5
    4. Molecular Formula:
    5. Molecular Weight: 276.4
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1360819-67-5.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: (Z)-3,3-dimethyl-1-(phenylthio)hexa-1,5-dien-2-yl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-3,3-dimethyl-1-(phenylthio)hexa-1,5-dien-2-yl acetate(1360819-67-5)
    11. EPA Substance Registry System: (Z)-3,3-dimethyl-1-(phenylthio)hexa-1,5-dien-2-yl acetate(1360819-67-5)

  • 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: 1360819-67-5(Hazardous Substances Data)

1360819-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360819-67-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,8,1 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1360819-67:
(9*1)+(8*3)+(7*6)+(6*0)+(5*8)+(4*1)+(3*9)+(2*6)+(1*7)=165
165 % 10 = 5
So 1360819-67-5 is a valid CAS Registry Number.

1360819-67-5Downstream Products

1360819-67-5Relevant articles and documents

A reactivity switch in the gold-catalysed coupling of allyl sulfides with propargylic carboxylates

Davies, Paul W.,Albrecht, Sebastien J.-C.

, p. 70 - 73 (2012)

The gold-catalysed coupling of allyl sulfides with propargylic carboxylates follows different pathways depending upon the choice of nonmigrating group on the sulfur and the aromatic group at the propargylic position of the alkyne substrate. Georg Thieme Verlag Stuttgart. New York.

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