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136859-86-4

(S)-2,2-dimethyl-1-(6-phenyl-pyridin-2-yl)propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 136859-86-4 Structure

  • Basic information

    1. Product Name: (S)-2,2-dimethyl-1-(6-phenyl-pyridin-2-yl)propanol
    2. Synonyms:
    3. CAS NO:136859-86-4
    4. Molecular Formula:
    5. Molecular Weight: 241.333
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136859-86-4.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: (S)-2,2-dimethyl-1-(6-phenyl-pyridin-2-yl)propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2,2-dimethyl-1-(6-phenyl-pyridin-2-yl)propanol(136859-86-4)
    11. EPA Substance Registry System: (S)-2,2-dimethyl-1-(6-phenyl-pyridin-2-yl)propanol(136859-86-4)

  • 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: 136859-86-4(Hazardous Substances Data)

136859-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136859-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,5 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136859-86:
(8*1)+(7*3)+(6*6)+(5*8)+(4*5)+(3*9)+(2*8)+(1*6)=174
174 % 10 = 4
So 136859-86-4 is a valid CAS Registry Number.

136859-86-4Downstream Products

136859-86-4Relevant articles and documents

Enantioselective Synthesis of Optically Active Pyridine Derivatives and C2-Symmetric 2,2'-Bipyridines

Bolm, Carsten,Ewald, Martina,Felder, Marcel,Schlingloff, Gunther

, p. 1169 - 1190 (2007/10/02)

Optically active pyridine derivatives 2, 15, 18, 19, 21, 26, and 27 are obtained by enantioselective reduction of the corresponding ketones 5, 7, 11-13, 24, and 25 using the chiral borane reagent chlorodiisopinocampherylborane .Nickel(0)-mediated coupling of bromopyridines 2, 15, and 31 gives C2-symmetric 2,2'-bipyridines (R,R)-32, (R,R)-33, and (S,S)-38, respectively, which form metal complexex with Co(II), Pd(II), Cu(I), and Ag(I).Aryl-substituted pyridines 26, and 39-41 are synthesized by palladium(0)-catalized cross coupling of 2 and 15 with boronic acids 42-44.Key Words: 2,2-Bipyridines / Pyridines, optically active / Chiral ligands / Asymmetric Synthesis / Catalysis, enantioselective

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