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CAS

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439574-61-5

N-(5-((5-(4-acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide is a complex chemical compound with potential pharmaceutical applications. It features a thiazole and benzamide ring connected by a linker containing a piperazine moiety. N-(5-((5-(4-acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide also includes a thioether and a methoxy group, as well as acetyl and methyl substituents. Its diverse structural features suggest that it may exhibit a range of biological activities, positioning it as a promising candidate for drug discovery and development.

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  • N-(5-((5-(4-acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide

    Cas No: 439574-61-5

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  • N-(5-((5-(4-acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide

    Cas No: 439574-61-5

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  • 439574-61-5 Structure

  • Basic information

    1. Product Name: N-(5-((5-(4-Acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide
    2. Synonyms: N-(5-((5-(4-Acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide;ITK inhibitor;BenzaMide, N-[5-[[5-[(4-acetyl-1-piperazinyl)carbonyl]-4-Methoxy-2-Methylphenyl]thio]-2-thiazolyl]-4-[[(1,2-diMethylpropyl)aMino]Methyl]-
    3. CAS NO:439574-61-5
    4. Molecular Formula: C31H39N5O4S2
    5. Molecular Weight: 609.80246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 439574-61-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.29
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 6.65±0.50(Predicted)
    10. CAS DataBase Reference: N-(5-((5-(4-Acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(5-((5-(4-Acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide(439574-61-5)
    12. EPA Substance Registry System: N-(5-((5-(4-Acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide(439574-61-5)

  • 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: 439574-61-5(Hazardous Substances Data)

439574-61-5 Usage

Uses

Used in Pharmaceutical Industry:
N-(5-((5-(4-acetylpiperazine-1-carbonyl)-4-methoxy-2-methylphenyl)thio)thiazol-2-yl)-4-(((3-methylbutan-2-yl)amino)methyl)benzamide is used as a potential drug candidate for various therapeutic applications due to its complex structure and diverse functional groups. Its specific biological activities and interactions with biological targets are yet to be fully explored, but its unique molecular architecture may offer novel therapeutic opportunities in treating various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 439574-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,5,7 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 439574-61:
(8*4)+(7*3)+(6*9)+(5*5)+(4*7)+(3*4)+(2*6)+(1*1)=185
185 % 10 = 5
So 439574-61-5 is a valid CAS Registry Number.

439574-61-5Downstream Products

439574-61-5Relevant articles and documents

Synthesis method for thiazole compound with tyrosine kinase inhibitory activity

-

, (2016/11/17)

The invention relates to a synthesis method for a thiazole compound (I) with tyrosine kinase inhibitory activity. Compound (3) and compound (II) react under the effect of a condensing agent, and thereby the compound (I) is obtained. The synthesis method i

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