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1268344-85-9

1-[(S)-2-hydroxy-1-(4-methoxyphenyl)ethyl]-4-methoxy-1H-pyrrol-2(5H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1268344-85-9 Structure

  • Basic information

    1. Product Name: 1-[(S)-2-hydroxy-1-(4-methoxyphenyl)ethyl]-4-methoxy-1H-pyrrol-2(5H)-one
    2. Synonyms: 1-[(S)-2-hydroxy-1-(4-methoxyphenyl)ethyl]-4-methoxy-1H-pyrrol-2(5H)-one
    3. CAS NO:1268344-85-9
    4. Molecular Formula:
    5. Molecular Weight: 263.293
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268344-85-9.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: 1-[(S)-2-hydroxy-1-(4-methoxyphenyl)ethyl]-4-methoxy-1H-pyrrol-2(5H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[(S)-2-hydroxy-1-(4-methoxyphenyl)ethyl]-4-methoxy-1H-pyrrol-2(5H)-one(1268344-85-9)
    11. EPA Substance Registry System: 1-[(S)-2-hydroxy-1-(4-methoxyphenyl)ethyl]-4-methoxy-1H-pyrrol-2(5H)-one(1268344-85-9)

  • 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: 1268344-85-9(Hazardous Substances Data)

1268344-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268344-85-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,3,4 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1268344-85:
(9*1)+(8*2)+(7*6)+(6*8)+(5*3)+(4*4)+(3*4)+(2*8)+(1*5)=179
179 % 10 = 9
So 1268344-85-9 is a valid CAS Registry Number.

1268344-85-9Relevant articles and documents

A flexible asymmetric approach to methyl 5-alkyltetramates and its application in the synthesis of cytotoxic marine natural product belamide A

Lan, Hong-Qiao,Ye, Jian-Liang,Wang, Ai-E,Ruan, Yuan-Ping,Huang, Pei-Qiang

experimental part, p. 958 - 968 (2011/03/20)

By using a methyl tetramate derivative (R)- or (S)-9 as a novel chiral building block, a direct, flexible, and highly enantioselective approach to methyl (R)- or (S)-5-alkyltetramates (2) is disclosed. Among the synthesized methyl 5-alkyltetramates 2, met

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