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CAS

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304895-28-1

N-[5-(4-methoxybenzyl)-1,3-thiazol-2-yl]heptanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 304895-28-1 Structure

  • Basic information

    1. Product Name: N-[5-(4-methoxybenzyl)-1,3-thiazol-2-yl]heptanamide
    2. Synonyms: N-[5-(4-methoxybenzyl)-1,3-thiazol-2-yl]heptanamide
    3. CAS NO:304895-28-1
    4. Molecular Formula: C18H24N2O2S
    5. Molecular Weight: 332.46036
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 304895-28-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.141±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.79±0.50(Predicted)
    10. CAS DataBase Reference: N-[5-(4-methoxybenzyl)-1,3-thiazol-2-yl]heptanamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-[5-(4-methoxybenzyl)-1,3-thiazol-2-yl]heptanamide(304895-28-1)
    12. EPA Substance Registry System: N-[5-(4-methoxybenzyl)-1,3-thiazol-2-yl]heptanamide(304895-28-1)

  • 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: 304895-28-1(Hazardous Substances Data)

304895-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 304895-28-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,8,9 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 304895-28:
(8*3)+(7*0)+(6*4)+(5*8)+(4*9)+(3*5)+(2*2)+(1*8)=151
151 % 10 = 1
So 304895-28-1 is a valid CAS Registry Number.

304895-28-1Downstream Products

304895-28-1Relevant articles and documents

Heterocyclic syntheses on the basis of arylation products of unsaturated compounds: X. 3-aryl-2-chloropropanals as reagents for the synthesis of 2-amino-1,3-thiazole derivatives

Obushak,Matiichuk,Vasylyshin,Ostapyuk

, p. 383 - 389 (2007/10/03)

Meerwein reaction of arenediazonium chlorides with acrolein gave 3-aryl-2-chloropropanals which were brought into cyclocondensation with thiourea. The resulting 2-amino-5-benzyl-1,3-thiazoles were acylated with carboxylic acid chlorides and phthalic anhydride to afford, respectively, 2-acylamino-5-benzyl-1,3-thiazoles and N-(5-benzyl-1,3-thiazol-2-yl) phthalimides.

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