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methyl 6-oxo-2-phenylhex-4-yn-3-yl carbonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1360733-40-9 Structure
  • Basic information

    1. Product Name: methyl 6-oxo-2-phenylhex-4-yn-3-yl carbonate
    2. Synonyms: methyl 6-oxo-2-phenylhex-4-yn-3-yl carbonate
    3. CAS NO:1360733-40-9
    4. Molecular Formula:
    5. Molecular Weight: 246.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1360733-40-9.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: methyl 6-oxo-2-phenylhex-4-yn-3-yl carbonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 6-oxo-2-phenylhex-4-yn-3-yl carbonate(1360733-40-9)
    11. EPA Substance Registry System: methyl 6-oxo-2-phenylhex-4-yn-3-yl carbonate(1360733-40-9)
  • 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: 1360733-40-9(Hazardous Substances Data)

1360733-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360733-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,7,3 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1360733-40:
(9*1)+(8*3)+(7*6)+(6*0)+(5*7)+(4*3)+(3*3)+(2*4)+(1*0)=139
139 % 10 = 9
So 1360733-40-9 is a valid CAS Registry Number.

1360733-40-9Upstream product

1360733-40-9Relevant articles and documents

N -heterocyclic carbene-catalyzed internal redox reaction of alkynals: An efficient synthesis of allenoates

Zhao, Yu-Ming,Tam, Yik,Wang, Yu-Jie,Li, Zigang,Sun, Jianwei

, p. 1398 - 1401 (2012/06/01)

An efficient N-heterocyclic carbene (NHC)-catalyzed internal redox reaction of alkynals that bear a γ leaving group has been developed. This process provides a new access to a range of allenoates in good yields. Preliminary results demonstrate that the en

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