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CAS

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478011-87-9

Ethanol, 2-[[(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]amino]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 478011-87-9 Structure

  • Basic information

    1. Product Name: Ethanol, 2-[[(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]amino]- (9CI)
    2. Synonyms: Ethanol, 2-[[(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]amino]- (9CI)
    3. CAS NO:478011-87-9
    4. Molecular Formula: C12H23NO
    5. Molecular Weight: 197.31712
    6. EINECS: N/A
    7. Product Categories: CYCLOPENTANE
    8. Mol File: 478011-87-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethanol, 2-[[(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]amino]- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanol, 2-[[(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]amino]- (9CI)(478011-87-9)
    11. EPA Substance Registry System: Ethanol, 2-[[(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]amino]- (9CI)(478011-87-9)

  • 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: 478011-87-9(Hazardous Substances Data)

478011-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478011-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,0,1 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 478011-87:
(8*4)+(7*7)+(6*8)+(5*0)+(4*1)+(3*1)+(2*8)+(1*7)=159
159 % 10 = 9
So 478011-87-9 is a valid CAS Registry Number.

478011-87-9Downstream Products

478011-87-9Relevant articles and documents

Enantiomerically enriched vic-amino alcohols from 2-iminobornanes

Squire, Michael D,Burwell, Amanda,Ferrence, Gregory M,Hitchcock, Shawn R

, p. 1849 - 1854 (2007/10/03)

Enantiomerically enriched vic-amino alcohols derived from D-camphor have been synthesized by condensation of the highly electrophilic N-nitroimine of D-camphor with ethanolamine, (R)-phenylglycinol and (1R,2S)-norephedrine to afford imines 8a-c. The imino

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