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1447966-55-3

2-{4-aminomethyl-2-[(phenylmethyl)amino]thiazol-5-yl}acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1447966-55-3 Structure

  • Basic information

    1. Product Name: 2-{4-aminomethyl-2-[(phenylmethyl)amino]thiazol-5-yl}acetic acid
    2. Synonyms: 2-{4-aminomethyl-2-[(phenylmethyl)amino]thiazol-5-yl}acetic acid
    3. CAS NO:1447966-55-3
    4. Molecular Formula:
    5. Molecular Weight: 277.347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1447966-55-3.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: 2-{4-aminomethyl-2-[(phenylmethyl)amino]thiazol-5-yl}acetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-{4-aminomethyl-2-[(phenylmethyl)amino]thiazol-5-yl}acetic acid(1447966-55-3)
    11. EPA Substance Registry System: 2-{4-aminomethyl-2-[(phenylmethyl)amino]thiazol-5-yl}acetic acid(1447966-55-3)

  • 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: 1447966-55-3(Hazardous Substances Data)

1447966-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1447966-55-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,9,6 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1447966-55:
(9*1)+(8*4)+(7*4)+(6*7)+(5*9)+(4*6)+(3*6)+(2*5)+(1*5)=213
213 % 10 = 3
So 1447966-55-3 is a valid CAS Registry Number.

1447966-55-3Downstream Products

1447966-55-3Relevant articles and documents

Synthesis of thiazole derivatives bearing an incorporated Z-5-aminopent-3-enoic acid fragment

Zavozin, Alexander G.,Ignat'Ev, Nikolai V.,Schulte, Michael,Zlotin, Sergei G.

, p. 6975 - 6980 (2013)

Novel compounds bearing a joint thiazole and a Z-5-aminopent-3-enoic acid fragments have been synthesized from readily accessible 5-bromolevulinic esters through a sequence of nucleophilic substitution, bromination, Hantzsch-type heterocyclization and Gabriel-like deprotection reactions. A majority of these reactions proceed in ionic liquid media that enhances their efficiency and selectivity in comparison to the corresponding reactions in conventional organic solvents. The compounds have a significant pharmaceutical potential.

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