Welcome to LookChem.com Sign In|Join Free

CAS

  • or
C16H18ClFN2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1041644-31-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1041644-31-8 Structure
  • Basic information

    1. Product Name: C16H18ClFN2O
    2. Synonyms:
    3. CAS NO:1041644-31-8
    4. Molecular Formula:
    5. Molecular Weight: 308.783
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1041644-31-8.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: C16H18ClFN2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H18ClFN2O(1041644-31-8)
    11. EPA Substance Registry System: C16H18ClFN2O(1041644-31-8)
  • 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: 1041644-31-8(Hazardous Substances Data)

1041644-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041644-31-8 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, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1041644-31:
(9*1)+(8*0)+(7*4)+(6*1)+(5*6)+(4*4)+(3*4)+(2*3)+(1*1)=108
108 % 10 = 8
So 1041644-31-8 is a valid CAS Registry Number.

1041644-31-8Downstream Products

1041644-31-8Relevant 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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1041644-31-8