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400088-55-3

2-cyano-N-pyridin-4-ylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 400088-55-3 Structure

  • Basic information

    1. Product Name: 2-cyano-N-pyridin-4-ylacetamide
    2. Synonyms: 2-cyano-N-pyridin-4-ylacetamide
    3. CAS NO:400088-55-3
    4. Molecular Formula: C8H7N3O
    5. Molecular Weight: 161.16068
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 400088-55-3.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: 2-cyano-N-pyridin-4-ylacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-cyano-N-pyridin-4-ylacetamide(400088-55-3)
    11. EPA Substance Registry System: 2-cyano-N-pyridin-4-ylacetamide(400088-55-3)

  • 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: 400088-55-3(Hazardous Substances Data)

400088-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 400088-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,0,8 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 400088-55:
(8*4)+(7*0)+(6*0)+(5*0)+(4*8)+(3*8)+(2*5)+(1*5)=103
103 % 10 = 3
So 400088-55-3 is a valid CAS Registry Number.

400088-55-3Downstream Products

400088-55-3Relevant articles and documents

Synthesis, cytotoxic characterization, and SAR study of imidazo[1,2-b]pyrazole-7-carboxamides

Demjén, András,Alf?ldi, Róbert,Angyal, Anikó,Gyuris, Márió,Hackler, László,Szebeni, Gábor J.,W?lfling, János,Puskás, László G.,Kanizsai, Iván

, (2018/07/13)

The synthesis and in vitro cytotoxic characteristics of new imidazo[1,2-b]pyrazole-7-carboxamides were investigated. Following a hit-to-lead optimization exploiting 2D and 3D cultures of MCF-7 human breast, 4T1 mammary gland, and HL-60 human promyelocytic leukemia cancer cell lines, a 67-membered library was constructed and the structure–activity relationship (SAR) was determined. Seven synthesized analogues exhibited sub-micromolar activities, from which compound 63 exerted the most significant potency with a remarkable HL-60 sensitivity (IC50 = 0.183 μM).

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