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1610691-86-5

(R)-N-[N-(2,2-dimethoxyethyl)glycinyl]-4-methoxyphenylalanine methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1610691-86-5 Structure

  • Basic information

    1. Product Name: (R)-N-[N-(2,2-dimethoxyethyl)glycinyl]-4-methoxyphenylalanine methyl ester
    2. Synonyms: (R)-N-[N-(2,2-dimethoxyethyl)glycinyl]-4-methoxyphenylalanine methyl ester
    3. CAS NO:1610691-86-5
    4. Molecular Formula:
    5. Molecular Weight: 354.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1610691-86-5.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)-N-[N-(2,2-dimethoxyethyl)glycinyl]-4-methoxyphenylalanine methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-N-[N-(2,2-dimethoxyethyl)glycinyl]-4-methoxyphenylalanine methyl ester(1610691-86-5)
    11. EPA Substance Registry System: (R)-N-[N-(2,2-dimethoxyethyl)glycinyl]-4-methoxyphenylalanine methyl ester(1610691-86-5)

  • 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: 1610691-86-5(Hazardous Substances Data)

1610691-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610691-86-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,6,9 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1610691-86:
(9*1)+(8*6)+(7*1)+(6*0)+(5*6)+(4*9)+(3*1)+(2*8)+(1*6)=155
155 % 10 = 5
So 1610691-86-5 is a valid CAS Registry Number.

1610691-86-5Downstream Products

1610691-86-5Relevant articles and documents

A diastereoselective construction of pyrazinoisoquinoline skeletons via tandem cyclization of phenylalanine derivatives: A facile synthesis of optically active pyrazinoisoquinolines

Seki, Maki,Ogiku, Tsuyoshi

, p. 3864 - 3870 (2014/06/09)

A facile and stereocontrolled construction of optically active pyrazinoisoquinoline skeletons based on tandem cyclization of enantiopure phenylalanine derivatives was examined. The reaction provided optically active 6,11b-trans pyrazinoisoquinoline ring systems in excellent diastereoselectivity, and this method was applicable to the cyclization of phenylalanine derivatives with diverse substituents.

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