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1443309-15-6

C22H19(2)H2N is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1443309-15-6 Structure

  • Basic information

    1. Product Name: C22H19(2)H2N
    2. Synonyms: C22H19(2)H2N
    3. CAS NO:1443309-15-6
    4. Molecular Formula:
    5. Molecular Weight: 301.4
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1443309-15-6.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: C22H19(2)H2N(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H19(2)H2N(1443309-15-6)
    11. EPA Substance Registry System: C22H19(2)H2N(1443309-15-6)

  • 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: 1443309-15-6(Hazardous Substances Data)

1443309-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1443309-15-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,3,0 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1443309-15:
(9*1)+(8*4)+(7*4)+(6*3)+(5*3)+(4*0)+(3*9)+(2*1)+(1*5)=136
136 % 10 = 6
So 1443309-15-6 is a valid CAS Registry Number.

1443309-15-6Upstream product

1443309-15-6Downstream Products

1443309-15-6Relevant articles and documents

Enantioselective iridium-catalyzed hydrogenation of 1- and 3-substituted isoquinolinium salts

Ye, Zhi-Shi,Guo, Ran-Ning,Cai, Xian-Feng,Chen, Mu-Wang,Shi, Lei,Zhou, Yong-Gui

supporting information, p. 3685 - 3689 (2013/04/24)

Asymmetric hydrogenation: The title reaction provides an efficient and rapid access to chiral 1- and 3-substituted 1,2,3,4-tetrahydroisoquinolines with excellent enantioselectivity (see scheme; L=ligand). A preliminary mechanistic study indicates that the 1,2-hydride addition might be the initial step in the reaction. The method has been used in the synthesis of urinary antispasmodic drug (+)-solifenacin. Copyright

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