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ethyl 2-amino-3-(2,5-dimethoxy-3,4-dimethylphenyl)propionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609636-45-4 Structure
  • Basic information

    1. Product Name: ethyl 2-amino-3-(2,5-dimethoxy-3,4-dimethylphenyl)propionate
    2. Synonyms: ethyl 2-amino-3-(2,5-dimethoxy-3,4-dimethylphenyl)propionate
    3. CAS NO:1609636-45-4
    4. Molecular Formula:
    5. Molecular Weight: 281.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609636-45-4.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: ethyl 2-amino-3-(2,5-dimethoxy-3,4-dimethylphenyl)propionate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-amino-3-(2,5-dimethoxy-3,4-dimethylphenyl)propionate(1609636-45-4)
    11. EPA Substance Registry System: ethyl 2-amino-3-(2,5-dimethoxy-3,4-dimethylphenyl)propionate(1609636-45-4)
  • 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: 1609636-45-4(Hazardous Substances Data)

1609636-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609636-45-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,6,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1609636-45:
(9*1)+(8*6)+(7*0)+(6*9)+(5*6)+(4*3)+(3*6)+(2*4)+(1*5)=184
184 % 10 = 4
So 1609636-45-4 is a valid CAS Registry Number.

1609636-45-4Relevant articles and documents

Synthesis of hexahydropyrazino[1,2-b]isoquinolines as simplified saframycin analogues

Nguyen Van, Tuyen,Claes, Pieter,De Kimpe, Norbert

supporting information, p. 69 - 74 (2014/01/06)

Various hexahydropyrazino[1,2-b]isoquinolines were synthesised as simplified saframycin analogues. Construction of this core proceeded through a tetrahydroisoquinoline synthesis followed by acylation/alkylation of the tetrahydroisoquinoline nitrogen and subsequent ring closure using various aliphatic and aromatic amines. The resulting piperazinones were reacted with LiAlH4 or LiAlH(OEt)3 to synthesise further analogues. Georg Thieme Verlag Stuttgart · New York.

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