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ethyl 2-(m-methoxyphenyl)-3-butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115981-96-9 Structure
  • Basic information

    1. Product Name: ethyl 2-(m-methoxyphenyl)-3-butanoate
    2. Synonyms: ethyl 2-(m-methoxyphenyl)-3-butanoate
    3. CAS NO:115981-96-9
    4. Molecular Formula:
    5. Molecular Weight: 433.286
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115981-96-9.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: ethyl 2-(m-methoxyphenyl)-3-butanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-(m-methoxyphenyl)-3-butanoate(115981-96-9)
    11. EPA Substance Registry System: ethyl 2-(m-methoxyphenyl)-3-butanoate(115981-96-9)
  • 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: 115981-96-9(Hazardous Substances Data)

115981-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115981-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,9,8 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115981-96:
(8*1)+(7*1)+(6*5)+(5*9)+(4*8)+(3*1)+(2*9)+(1*6)=149
149 % 10 = 9
So 115981-96-9 is a valid CAS Registry Number.

115981-96-9Relevant articles and documents

Effects of Addition of a 2-Methyl Group to Ethyl Nipecotates (β-Meperidines) on Receptor Affinities and Opiate Agonist/Antagonist Activities

Lawson, John A.,Cheng, Alice,DeGraw, Joseph,Frenking, Gernot,Uyeno, Edward,et al.

, p. 2015 - 2021 (2007/10/02)

A series of 2-methyl-3-carbethoxy-3-(m-hydroxyphenyl)piperidine opiates (13a-d) with N-substituent variations have been synthesized, and their receptor affinities and in vivo agonist and antagonist activities and energy-conformational profiles have been d

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