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CAS

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1363334-16-0

Diisopropyl(6,7-dimethoxy-2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1363334-16-0 Structure

  • Basic information

    1. Product Name: Diisopropyl(6,7-dimethoxy-2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate
    2. Synonyms: Diisopropyl(6,7-dimethoxy-2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate
    3. CAS NO:1363334-16-0
    4. Molecular Formula:
    5. Molecular Weight: 433.485
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1363334-16-0.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: Diisopropyl(6,7-dimethoxy-2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Diisopropyl(6,7-dimethoxy-2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate(1363334-16-0)
    11. EPA Substance Registry System: Diisopropyl(6,7-dimethoxy-2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate(1363334-16-0)

  • 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: 1363334-16-0(Hazardous Substances Data)

1363334-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1363334-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,3,3 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1363334-16:
(9*1)+(8*3)+(7*6)+(6*3)+(5*3)+(4*3)+(3*4)+(2*1)+(1*6)=140
140 % 10 = 0
So 1363334-16-0 is a valid CAS Registry Number.

1363334-16-0Downstream Products

1363334-16-0Relevant articles and documents

Molybdenum trioxide catalyzed oxidative cross-dehydrogenative coupling of benzylic sp3 C-H bonds: Synthesis of α-aminophosphonates under aerobic conditions

Alagiri, Kaliyamoorthy,Devadig, Pradeep,Prabhu, Kandikere R.

, p. 1456 - 1459 (2012)

Molybdenum trioxide (MoO3) catalyzed efficient oxidative cross-dehydrogenative-coupling (CDC) method for C-H functionalization of N-aryl tetrahydroisoquinolines has been explored. This user-friendly method of synthesizing α-aminophosphonates employs 1.1 equiv of dialkyl-H- phosphonate under aerobic condition. Formation of new C-P bonds from unfunctionalized starting materials under environmentally benign conditions provides an excellent avenue for the synthesis of biologically active α-aminophosphonates.

CDC reactions of N-aryl tetrahydroisoquinolines using catalytic amounts of DDQ: C-H activation under aerobic conditions

Alagiri, Kaliyamoorthy,Devadig, Pradeep,Prabhu, Kandikere R.

supporting information; experimental part, p. 5160 - 5164 (2012/05/20)

An oxidative cross-dehydrogenative coupling (CDC) reaction for the formation of C-C and C-P bonds is disclosed using a catalytic amount of DDQ (10 mol %) under aerobic conditions (see scheme). This unprecedented environmentally benign strategy of using AI

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