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351015-76-4

2-(3-formylindol-1-yl)-3-methylbutyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 351015-76-4 Structure

  • Basic information

    1. Product Name: 2-(3-formylindol-1-yl)-3-methylbutyric acid
    2. Synonyms: 2-(3-formylindol-1-yl)-3-methylbutyric acid
    3. CAS NO:351015-76-4
    4. Molecular Formula: C14H15NO3
    5. Molecular Weight: 245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 351015-76-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(3-formylindol-1-yl)-3-methylbutyric acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-formylindol-1-yl)-3-methylbutyric acid(351015-76-4)
    11. EPA Substance Registry System: 2-(3-formylindol-1-yl)-3-methylbutyric acid(351015-76-4)

  • 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: 351015-76-4(Hazardous Substances Data)

351015-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 351015-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,0,1 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 351015-76:
(8*3)+(7*5)+(6*1)+(5*0)+(4*1)+(3*5)+(2*7)+(1*6)=104
104 % 10 = 4
So 351015-76-4 is a valid CAS Registry Number.

351015-76-4Downstream Products

351015-76-4Relevant articles and documents

Synthesis of 1-Substituted Indole-3-carboxaldehydes Related to Acyclic Nucleosides and Their Condensed Pyrenyl Derivatives

Zahran, Magdy A.,Afify, Hanan M.,Pedersen, Erik B.,Nielsen, Claus

, p. 101 - 114 (2007/10/03)

Indole-3-carboxaldehyde was N-alkylated to give the corresponding acyclic nucleosides 3a-h which were condensed with 1-pyrenamine and 1-acetylpyrene to give 5a,c,e-g and 7b-d,e,g, respectively. The Schiff's bases 5a and 5e with 2-hydroxyethyl and methylthiomethyl N-1-substituents were found moderate active against HIV-1.

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