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2-((1R,2R,4S)-7-tert-Butoxy-bicyclo[2.2.1]hept-5-en-2-yloxy)-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100509-01-1 Structure
  • Basic information

    1. Product Name: 2-((1R,2R,4S)-7-tert-Butoxy-bicyclo[2.2.1]hept-5-en-2-yloxy)-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole
    2. Synonyms:
    3. CAS NO:100509-01-1
    4. Molecular Formula:
    5. Molecular Weight: 355.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100509-01-1.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-((1R,2R,4S)-7-tert-Butoxy-bicyclo[2.2.1]hept-5-en-2-yloxy)-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((1R,2R,4S)-7-tert-Butoxy-bicyclo[2.2.1]hept-5-en-2-yloxy)-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole(100509-01-1)
    11. EPA Substance Registry System: 2-((1R,2R,4S)-7-tert-Butoxy-bicyclo[2.2.1]hept-5-en-2-yloxy)-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole(100509-01-1)
  • 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: 100509-01-1(Hazardous Substances Data)

100509-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100509-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,0 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100509-01:
(8*1)+(7*0)+(6*0)+(5*5)+(4*0)+(3*9)+(2*0)+(1*1)=61
61 % 10 = 1
So 100509-01-1 is a valid CAS Registry Number.

100509-01-1Downstream Products

100509-01-1Relevant articles and documents

REACTION OF t-BUTOXY RADICALS WITH NORBORNADIENE

Busfield, Ken W.,Jenkins, Ian D.,Thang, San H.,Rizzardo, Ezio,Solomon, David H.

, p. 5081 - 5084 (1985)

95 percent of the reaction of t-butoxy radicals with norbornadiene occurs by radical addition followed by rearrangement to nortricyclyl and 7-t-butoxynorbornenyl products; the remainder includes a novel radical rearragement involving a 1,3-H shift and some radical abstraction observed for the first time.

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