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CAS

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41801-97-2

Oxirane, 3-methyl-2-(1-naphthalenyl)-2-phenyl-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 41801-97-2 Structure

  • Basic information

    1. Product Name: Oxirane, 3-methyl-2-(1-naphthalenyl)-2-phenyl-, cis-
    2. Synonyms:
    3. CAS NO:41801-97-2
    4. Molecular Formula: C19H16O
    5. Molecular Weight: 260.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41801-97-2.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: Oxirane, 3-methyl-2-(1-naphthalenyl)-2-phenyl-, cis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Oxirane, 3-methyl-2-(1-naphthalenyl)-2-phenyl-, cis-(41801-97-2)
    11. EPA Substance Registry System: Oxirane, 3-methyl-2-(1-naphthalenyl)-2-phenyl-, cis-(41801-97-2)

  • 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: 41801-97-2(Hazardous Substances Data)

41801-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41801-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,0 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41801-97:
(7*4)+(6*1)+(5*8)+(4*0)+(3*1)+(2*9)+(1*7)=102
102 % 10 = 2
So 41801-97-2 is a valid CAS Registry Number.

41801-97-2Downstream Products

41801-97-2Relevant articles and documents

Mechanisms of Epoxidation during Ozonation of Carbon-Carbon Double Bonds

Bailey, Philip S.,Hwang, Hank H.,Chiang, Chin-Yun

, p. 231 - 234 (2007/10/02)

Epoxidation of several highly hindered olefins with ozone is stereospecific in all solvents, nucleophilic or nonnucleophilic.This is in agreement with expectations based on the initial formation of a ? rather than an open ? complex.

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