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1026599-79-0

[1-(3,4-dimethoxy-phenyl)-propyl]-carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1026599-79-0 Structure

  • Basic information

    1. Product Name: [1-(3,4-dimethoxy-phenyl)-propyl]-carbamic acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:1026599-79-0
    4. Molecular Formula:
    5. Molecular Weight: 295.379
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1026599-79-0.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: [1-(3,4-dimethoxy-phenyl)-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: [1-(3,4-dimethoxy-phenyl)-propyl]-carbamic acid tert-butyl ester(1026599-79-0)
    11. EPA Substance Registry System: [1-(3,4-dimethoxy-phenyl)-propyl]-carbamic acid tert-butyl ester(1026599-79-0)

  • 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: 1026599-79-0(Hazardous Substances Data)

1026599-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026599-79-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,5,9 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1026599-79:
(9*1)+(8*0)+(7*2)+(6*6)+(5*5)+(4*9)+(3*9)+(2*7)+(1*9)=170
170 % 10 = 0
So 1026599-79-0 is a valid CAS Registry Number.

1026599-79-0Downstream Products

1026599-79-0Relevant articles and documents

A new general method for the asymmetric synthesis of 4-alkyl-3-aryl- 1,2,3,4-tetrahydroisoquinolines

Vicario, Jose L.,Badia, Dolores,Dominguez, Esther,Carrillo, Luisa

, p. 4610 - 4616 (2007/10/03)

A highly enantioselective method for the synthesis of 4-alkyl substituted 1,2,3,4-tetrahydroisoquinolines is reported. The key step relies on the asymmetric synthesis of α-alkylarylacetic acids by alkylation of their corresponding amides employing (S,S)-(+)-pseudoephedrine as chiral inductor. Subsequent Friedel-Crafts acylation, stereocontrolled reductive amination and Pictet-Spengler cyclization affords the title compounds in excellent yields and enantioselectivities.

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