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Isoquinolin-1-ylMethyl-Methyl-aMine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144163-92-8 Structure
  • Basic information

    1. Product Name: Isoquinolin-1-ylMethyl-Methyl-aMine
    2. Synonyms: Isoquinolin-1-ylMethyl-Methyl-aMine;1-(isoquinolin-1-yl)-N-methylmethanamine
    3. CAS NO:144163-92-8
    4. Molecular Formula: C11H12N2
    5. Molecular Weight: 172.22638
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144163-92-8.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: Isoquinolin-1-ylMethyl-Methyl-aMine(CAS DataBase Reference)
    10. NIST Chemistry Reference: Isoquinolin-1-ylMethyl-Methyl-aMine(144163-92-8)
    11. EPA Substance Registry System: Isoquinolin-1-ylMethyl-Methyl-aMine(144163-92-8)
  • 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: 144163-92-8(Hazardous Substances Data)

144163-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144163-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,6 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144163-92:
(8*1)+(7*4)+(6*4)+(5*1)+(4*6)+(3*3)+(2*9)+(1*2)=118
118 % 10 = 8
So 144163-92-8 is a valid CAS Registry Number.

144163-92-8Downstream Products

144163-92-8Relevant articles and documents

Base-Promoted Tandem Synthesis of 2-Azaaryl Tetrahydroquinolines

Chen, Shuguang,Yang, Langxuan,Shang, Yongjia,Mao, Jianyou,Walsh, Patrick J.

supporting information, p. 1594 - 1599 (2021/03/08)

A novel method to synthesize 2-azaaryl tetrahydroquinolines by the base-promoted tandem reaction of azaaryl methyl amines and styrene derivatives is reported (over 30 examples, yields up to 95%). Mechanistic probe experiments demonstrate that the deprotonation of the benzylic C-H bond and the addition to the styrene vinyl group proceeds via the SNAr mechanism.

Introduction of Quinolines and Isoquinolines onto Nonactivated α-C-H Bond of Tertiary Amides through a Radical Pathway

Okugawa, Naoki,Moriyama, Katsuhiko,Togo, Hideo

, p. 170 - 178 (2017/04/26)

Treatment of quinolines and isoquinolines with benzoyl peroxide in tertiary amides, such as N,N-dimethylacetamide, N,N-dimethylpropionamide, and N-acetylpyrrolidine, etc., under irradiation with a Hg lamp in the temperature range of 35 °C to 40 °C gave C-C-bonded quinolines and isoquinolines bearing amide groups with high regioselectivity in good to moderate yields, respectively, under transition-metal-free conditions.

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