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130442-63-6

2,2-Dimethyl-1-(p-tolyl)bicyclo<1.1.0>butan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130442-63-6 Structure

  • Basic information

    1. Product Name: 2,2-Dimethyl-1-(p-tolyl)bicyclo<1.1.0>butan
    2. Synonyms:
    3. CAS NO:130442-63-6
    4. Molecular Formula:
    5. Molecular Weight: 172.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130442-63-6.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: 2,2-Dimethyl-1-(p-tolyl)bicyclo<1.1.0>butan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-Dimethyl-1-(p-tolyl)bicyclo<1.1.0>butan(130442-63-6)
    11. EPA Substance Registry System: 2,2-Dimethyl-1-(p-tolyl)bicyclo<1.1.0>butan(130442-63-6)

  • 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: 130442-63-6(Hazardous Substances Data)

130442-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130442-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,4 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130442-63:
(8*1)+(7*3)+(6*0)+(5*4)+(4*4)+(3*2)+(2*6)+(1*3)=86
86 % 10 = 6
So 130442-63-6 is a valid CAS Registry Number.

130442-63-6Relevant articles and documents

PHOTOOXYGENIERUNG VON 1-ARYL-2,2-DIMETHYLBICYCLOBUTANEN

Gollnick, Klaus,Weber, Maria

, p. 4585 - 4588 (2007/10/02)

Oxygenations of highly strained 1-phenyl- (5a) and 1-(p-tolyl)-substituted 2,2-dimethylbicyclobutanes (5b), photosensitized by 9,10-dicyanoanthracene in acetonitrile, yield about 90 percent of 1-phenyl- (6a) and 1-(p-tolyl)-substituted 3,4-epoxy-4-methyl-1-pentanones (6b), and about 10 percent of 3-phenyl- (7a) and 3-(p-tolyl)-substituted 3,4-epoxy-4-methylpentanals (7b), respectively.Evidence is presented that ketones 6a,b are formed by an electron-transfer induced process, whereas aldehydes 7a,b are generated by a singlet-oxygen reaction.

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