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  • 874278-06-5 Structure
  • Basic information

    1. Product Name: C27H33N5S
    2. Synonyms:
    3. CAS NO:874278-06-5
    4. Molecular Formula:
    5. Molecular Weight: 459.659
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 874278-06-5.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: C27H33N5S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C27H33N5S(874278-06-5)
    11. EPA Substance Registry System: C27H33N5S(874278-06-5)
  • 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: 874278-06-5(Hazardous Substances Data)

874278-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874278-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,2,7 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 874278-06:
(8*8)+(7*7)+(6*4)+(5*2)+(4*7)+(3*8)+(2*0)+(1*6)=205
205 % 10 = 5
So 874278-06-5 is a valid CAS Registry Number.

874278-06-5Downstream Products

874278-06-5Relevant articles and documents

Small molecule antagonists of the gonadotropin-releasing hormone (GnRH) receptor: Structure-activity relationships of small heterocyclic groups appended to the 2-phenyl-4-piperazinyl-benzimidazole template

Hauze, Diane B.,Chengalvala, Murty V.,Cottom, Joshua E.,Feingold, Irene B.,Garrick, Lloyd,Green, Daniel M.,Huselton, Christine,Kao, Wenling,Kees, Kenneth,Lundquist IV, Joseph T.,Mann, Charles W.,Mehlmann, John F.,Rogers, John F.,Shanno, Linda,Wrobel, Jay,Pelletier, Jeffrey C.

scheme or table, p. 1986 - 1990 (2009/11/30)

A previous report described the serum LH suppression pharmacology of the 2-phenyl-4-piperazinyl-benzimidazole N-ethyluracil GnRH receptor antagonist 1 following oral administration in rats. A series of small heterocycles were appended to the 2-(4-tert-but

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