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515174-13-7

tert-butyl 3.5-dimethyl-4-nirtobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 515174-13-7 Structure

  • Basic information

    1. Product Name: tert-butyl 3.5-dimethyl-4-nirtobenzoate
    2. Synonyms: tert-butyl 3.5-dimethyl-4-nirtobenzoate
    3. CAS NO:515174-13-7
    4. Molecular Formula: C13H17NO4
    5. Molecular Weight: 251.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 515174-13-7.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: tert-butyl 3.5-dimethyl-4-nirtobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 3.5-dimethyl-4-nirtobenzoate(515174-13-7)
    11. EPA Substance Registry System: tert-butyl 3.5-dimethyl-4-nirtobenzoate(515174-13-7)

  • 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: 515174-13-7(Hazardous Substances Data)

515174-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 515174-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,5,1,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 515174-13:
(8*5)+(7*1)+(6*5)+(5*1)+(4*7)+(3*4)+(2*1)+(1*3)=127
127 % 10 = 7
So 515174-13-7 is a valid CAS Registry Number.

515174-13-7Relevant articles and documents

Synthesis and binding studies of bowl-shaped hosts for quaternary ammoniums

Jeong, Kyu-Sung,Shin, Kwang Hoon,Kim, Soong-Hyun

, p. 1166 - 1167 (2007/10/03)

Two bowl-shaped hosts for quaternary ammonium salts were synthesized and their binding properties, along with the anion effect, were systematically examined and compared in CDCl3.

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