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  • 1191401-02-1 Structure
  • Basic information

    1. Product Name: N-pyridazin-3-yl-4-[3-(tetrahydro-2H-pyran-2-ylmethoxy)benzylidene]piperidine-1-carboxamide
    2. Synonyms: N-pyridazin-3-yl-4-[3-(tetrahydro-2H-pyran-2-ylmethoxy)benzylidene]piperidine-1-carboxamide
    3. CAS NO:1191401-02-1
    4. Molecular Formula:
    5. Molecular Weight: 408.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1191401-02-1.mol
    9. Article Data: 1
  • 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: N-pyridazin-3-yl-4-[3-(tetrahydro-2H-pyran-2-ylmethoxy)benzylidene]piperidine-1-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-pyridazin-3-yl-4-[3-(tetrahydro-2H-pyran-2-ylmethoxy)benzylidene]piperidine-1-carboxamide(1191401-02-1)
    11. EPA Substance Registry System: N-pyridazin-3-yl-4-[3-(tetrahydro-2H-pyran-2-ylmethoxy)benzylidene]piperidine-1-carboxamide(1191401-02-1)
  • 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: 1191401-02-1(Hazardous Substances Data)

1191401-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1191401-02-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,1,4,0 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1191401-02:
(9*1)+(8*1)+(7*9)+(6*1)+(5*4)+(4*0)+(3*1)+(2*0)+(1*2)=111
111 % 10 = 1
So 1191401-02-1 is a valid CAS Registry Number.

1191401-02-1Downstream Products

1191401-02-1Relevant articles and documents

ETHER BENZYLIDENE PIPERIDINE ARYL CARBOXAMIDE COMPOUNDS USEFUL AS FAAH INHIBITORS

-

, (2009/12/02)

The present invention relates to compounds of Formula (I) wherein Ar is optionally substituted phenyl or 6-membered heteroaryl moiety, or a benzisoxazole, pyrrolopyridine, or benzotriazole group; or a pharmaceutically acceptable salt thereof; processes for the preparation of the compounds; intermediates used in the preparation of the compounds; compositions containing the compounds; and uses of the compounds in treating diseases or conditions associated with fatty acid amide hydrolase (FAAH) activity, including pain, urinary incontinence, overactive bladder, emesis, cognitive disorders, anxiety, depression, sleeping disorders, eating disorders, movement disorders, glaucoma, psoriasis, multiple sclerosis, cerebrovascular disorders, brain injury, gastrointestinal disorders, hypertension, or cardiovascular disease.

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