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146530-34-9

(R)-2-formyl-1,2,3,4-tetrahydro-3-phenylisoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146530-34-9 Structure

  • Basic information

    1. Product Name: (R)-2-formyl-1,2,3,4-tetrahydro-3-phenylisoquinoline
    2. Synonyms:
    3. CAS NO:146530-34-9
    4. Molecular Formula:
    5. Molecular Weight: 237.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146530-34-9.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: (R)-2-formyl-1,2,3,4-tetrahydro-3-phenylisoquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-formyl-1,2,3,4-tetrahydro-3-phenylisoquinoline(146530-34-9)
    11. EPA Substance Registry System: (R)-2-formyl-1,2,3,4-tetrahydro-3-phenylisoquinoline(146530-34-9)

  • 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: 146530-34-9(Hazardous Substances Data)

146530-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146530-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,3 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146530-34:
(8*1)+(7*4)+(6*6)+(5*5)+(4*3)+(3*0)+(2*3)+(1*4)=119
119 % 10 = 9
So 146530-34-9 is a valid CAS Registry Number.

146530-34-9Relevant articles and documents

Use of the N-formyliminium ion cyclization for the synthesis of 3-aryl-1,2,3,4-tetrahydroisoquinolines

Maryanoff,Rebarchak

, p. 1245 - 1248 (2007/10/02)

Classical cyclization procedures for the synthesis of 3-arylisoquinolines are fraught with complications. Here, we present the application of an N-acyliminium cyclization to such target molecules. N(1,2-diarylethyl)formamides 1, 4a-4d, and 4f were cyclize

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