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CAS

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64890-04-6

3-Oxa-1-azabicyclo[3.1.0]hexan-2-one, 4,4,5-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64890-04-6 Structure

  • Basic information

    1. Product Name: 3-Oxa-1-azabicyclo[3.1.0]hexan-2-one, 4,4,5-triphenyl-
    2. Synonyms:
    3. CAS NO:64890-04-6
    4. Molecular Formula: C22H17NO2
    5. Molecular Weight: 327.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64890-04-6.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: 3-Oxa-1-azabicyclo[3.1.0]hexan-2-one, 4,4,5-triphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Oxa-1-azabicyclo[3.1.0]hexan-2-one, 4,4,5-triphenyl-(64890-04-6)
    11. EPA Substance Registry System: 3-Oxa-1-azabicyclo[3.1.0]hexan-2-one, 4,4,5-triphenyl-(64890-04-6)

  • 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: 64890-04-6(Hazardous Substances Data)

64890-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64890-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,9 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64890-04:
(7*6)+(6*4)+(5*8)+(4*9)+(3*0)+(2*0)+(1*4)=146
146 % 10 = 6
So 64890-04-6 is a valid CAS Registry Number.

64890-04-6Relevant articles and documents

Reaction of (2-ethyl-aziridin-2-yl)diphenyl methanol and diphenyl-(2-phenyl-aziridin-2-yl)methanol with phenyl and t-butyl isocyanates, phenyl isothiocyanate and thiophosgene

Kryczka,Lesniak,Pasternak,Porwanski

, p. 1927 - 1934 (2008/09/18)

The reactions of aziridine alcohols with organic isocyanates, isothiocyanates and thiophosgene were described. It was found that the reactions with phenyl or t-butyl isocyanate give urea derivatives as major products, whereas the reaction with thiophosgene resulted in the formation of isothiocyanates derivatives. The mechanism of these reactions was proposed.

SYNTHESE PHOTOCHIMIQUE D'AZA-1 BICYCLOBUTANES

Bartnik, Romuald,Cebulska, Zofia,Laurent, Andre

, p. 4197 - 4198 (2007/10/02)

Aza-1 bicyclobutanes 2 are readily obtained by photolysis of carbamates 1. 1 are easily synthetised from 3.

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