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511243-61-1

(2-dimethylaminophenyl)dicyclohexylmethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 511243-61-1 Structure

  • Basic information

    1. Product Name: (2-dimethylaminophenyl)dicyclohexylmethanol
    2. Synonyms: (2-dimethylaminophenyl)dicyclohexylmethanol
    3. CAS NO:511243-61-1
    4. Molecular Formula:
    5. Molecular Weight: 315.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 511243-61-1.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-dimethylaminophenyl)dicyclohexylmethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-dimethylaminophenyl)dicyclohexylmethanol(511243-61-1)
    11. EPA Substance Registry System: (2-dimethylaminophenyl)dicyclohexylmethanol(511243-61-1)

  • 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: 511243-61-1(Hazardous Substances Data)

511243-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 511243-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,2,4 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 511243-61:
(8*5)+(7*1)+(6*1)+(5*2)+(4*4)+(3*3)+(2*6)+(1*1)=101
101 % 10 = 1
So 511243-61-1 is a valid CAS Registry Number.

511243-61-1Relevant articles and documents

Synthesis and molecular structures of (2-dialkylaminophenyl)alcohols and of 2-phenylaminoalkyl-dimethylaminobenzene derivatives

Al-Masri, Harbi Tomah,Sieler, Joachim,L?nnecke, Peter,Blaurock, Steffen,Domasevitch, Konstantin,Hey-Hawkins, Evamarie

, p. 333 - 339 (2007/10/03)

N,N-Dimethyl-o-toluidine, N,N-dimethylaniline, and N,N-diethylaniline were treated with n-butyllithium-tmeda in diethyl ether-hexane solution to give o-lithioarylamines, which react with various electrophiles (benzophenone, dicyclohexyl ketone, benzaldehy

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