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  • 1041644-40-9 Structure
  • Basic information

    1. Product Name: C14H11ClFN3O
    2. Synonyms:
    3. CAS NO:1041644-40-9
    4. Molecular Formula:
    5. Molecular Weight: 291.712
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1041644-40-9.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: C14H11ClFN3O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H11ClFN3O(1041644-40-9)
    11. EPA Substance Registry System: C14H11ClFN3O(1041644-40-9)
  • 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: 1041644-40-9(Hazardous Substances Data)

1041644-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041644-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,6,4 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1041644-40:
(9*1)+(8*0)+(7*4)+(6*1)+(5*6)+(4*4)+(3*4)+(2*4)+(1*0)=109
109 % 10 = 9
So 1041644-40-9 is a valid CAS Registry Number.

1041644-40-9Downstream Products

1041644-40-9Relevant articles and documents

Structure-activity relationship and liver microsome stability studies of pyrrole necroptosis inhibitors

Teng, Xin,Keys, Heather,Yuan, Junying,Degterev, Alexei,Cuny, Gregory D.

body text, p. 3219 - 3223 (2009/04/06)

Necroptosis is a regulated caspase-independent cell death pathway resulting in morphology reminiscent of passive non-regulated necrosis. Several diverse structure classes of necroptosis inhibitors have been reported to date, including a series of [1,2,3]thiadiazole benzylamide derivatives. However, initial evaluation of mouse liver microsome stability indicated that this series of compounds was rapidly degraded. A structure-activity relationship (SAR) study of the [1,2,3]thiadiazole benzylamide series revealed that increased mouse liver microsome stability and increased necroptosis inhibitory activity could be accomplished by replacement of the 4-cyclopropyl-[1,2,3]thiadiazole with a 5-cyano-1-methylpyrrole. In addition, the SAR and the cellular activity profiles, utilizing different cell types and necroptosis-inducing stimuli, of representative [1,2,3]thiadiazole and pyrrole derivatives were very similar suggesting that the two compound series inhibit necroptosis in the same manner.

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