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1159977-12-4

rac N-Boc-anatabine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1159977-12-4 Structure

  • Basic information

    1. Product Name: rac N-Boc-anatabine
    2. Synonyms: rac N-Boc-anatabine;3,6-Dihydro-[2,3'-bipyridine]-1(2H)-carboxylic Acid 1,1-DiMethylethyl Ester
    3. CAS NO:1159977-12-4
    4. Molecular Formula: C15H20N2O2
    5. Molecular Weight: 260.3315
    6. EINECS: N/A
    7. Product Categories: Aromatics;Heterocycles;Intermediates;Nicotine Derivatives;Aromatics, Heterocycles, Intermediates, Nicotine Derivatives
    8. Mol File: 1159977-12-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 364.5±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.105±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 5.06±0.12(Predicted)
    10. CAS DataBase Reference: rac N-Boc-anatabine(CAS DataBase Reference)
    11. NIST Chemistry Reference: rac N-Boc-anatabine(1159977-12-4)
    12. EPA Substance Registry System: rac N-Boc-anatabine(1159977-12-4)

  • 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: 1159977-12-4(Hazardous Substances Data)

1159977-12-4 Usage

Chemical Properties

Yellow Oil

Uses

Anatabine (A637500) derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 1159977-12-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,9,7 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1159977-12:
(9*1)+(8*1)+(7*5)+(6*9)+(5*9)+(4*7)+(3*7)+(2*1)+(1*2)=204
204 % 10 = 4
So 1159977-12-4 is a valid CAS Registry Number.

1159977-12-4Downstream Products

1159977-12-4Relevant articles and documents

A Practical and Efficient Synthesis of (±)-Anatabine

Rossi, Federico V.,Ballini, Roberto,Barboni, Luciano,Allegrini, Pietro,Palmieri, Alessandro

, p. 1921 - 1925 (2018)

A new efficient synthesis of racemic anatabine is reported. The title target was obtained in an excellent overall yield of 70%, by a five-step synthesis, using cheap reagents and mild reaction conditions.

Preparation method for anatabine

-

Paragraph 0021; 0027; 0028; 0036; 0037; 0045; 0046, (2017/11/04)

The invention discloses a preparation method for anatabine. The method comprises the steps of (1) enabling 3-amino methyl pyridine to react with benzophenone to obtain an intermediate 1; (2) synthesizing an intermediate 2 by the intermediate 1 and cis-1,4-dichloro-2-butene; (3) enabling the intermediate 2 to react with Boc anhydride to obtain an intermediate 3; and (4) removing a Boc group from the intermediate 3 to obtain an intermediate 4 to obtain an anatabine product. The anatabine prepared by adopting the method is high in yield, high in purity and good in quality.

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