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CAS

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53059-45-3

methyl 2-<α-<(tert-butyl)amino>benzyl>prop-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53059-45-3 Structure

  • Basic information

    1. Product Name: methyl 2-<α-<(tert-butyl)amino>benzyl>prop-2-enoate
    2. Synonyms: methyl 2-<α-<(tert-butyl)amino>benzyl>prop-2-enoate
    3. CAS NO:53059-45-3
    4. Molecular Formula:
    5. Molecular Weight: 247.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53059-45-3.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: methyl 2-<α-<(tert-butyl)amino>benzyl>prop-2-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-<α-<(tert-butyl)amino>benzyl>prop-2-enoate(53059-45-3)
    11. EPA Substance Registry System: methyl 2-<α-<(tert-butyl)amino>benzyl>prop-2-enoate(53059-45-3)

  • 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: 53059-45-3(Hazardous Substances Data)

53059-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53059-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53059-45:
(7*5)+(6*3)+(5*0)+(4*5)+(3*9)+(2*4)+(1*5)=113
113 % 10 = 3
So 53059-45-3 is a valid CAS Registry Number.

53059-45-3Relevant articles and documents

115. α-Methylidene-and α-alkylidene-β-lactams from nonproteinogenic amino acids

Buchholz, Rainer,Hoffmann, H. Martin R.

, p. 1213 - 1220 (2015/01/08)

Treatment of methyl 2-(l-hydroxyalkyl)prop-2-enoates1 with conc. HBr solution afforded methyl (Z)-2-(bromomethyl)alk-2-enoates 2, which were transformed regioselectively into N-substituted methyl (E)-2-(aminomethyl)alk-2-enoates 3 (SN2 reaction

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