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470477-62-4

3-chloro-4-(1-cyclopentylpiperidin-4-yloxy)nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 470477-62-4 Structure

  • Basic information

    1. Product Name: 3-chloro-4-(1-cyclopentylpiperidin-4-yloxy)nitrobenzene
    2. Synonyms: 3-chloro-4-(1-cyclopentylpiperidin-4-yloxy)nitrobenzene
    3. CAS NO:470477-62-4
    4. Molecular Formula:
    5. Molecular Weight: 324.807
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 470477-62-4.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: 3-chloro-4-(1-cyclopentylpiperidin-4-yloxy)nitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-chloro-4-(1-cyclopentylpiperidin-4-yloxy)nitrobenzene(470477-62-4)
    11. EPA Substance Registry System: 3-chloro-4-(1-cyclopentylpiperidin-4-yloxy)nitrobenzene(470477-62-4)

  • 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: 470477-62-4(Hazardous Substances Data)

470477-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 470477-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,4,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 470477-62:
(8*4)+(7*7)+(6*0)+(5*4)+(4*7)+(3*7)+(2*6)+(1*2)=164
164 % 10 = 4
So 470477-62-4 is a valid CAS Registry Number.

470477-62-4Relevant articles and documents

Discovery of R-142086 as a factor Xa (FXa) inhibitor: Syntheses and structure-activity relationships of cinnamyl derivatives1,2

Noguchi, Tetsuji,Tanaka, Naoki,Nishimata, Toyoki,Goto, Riki,Hayakawa, Miho,Sugidachi, Atsuhiro,Ogawa, Taketoshi,Niitsu, Yoichi,Asai, Fumitoshi,Ishizuka, Tomoko,Fujimoto, Koichi

experimental part, p. 22 - 33 (2009/08/07)

To develop a novel and effective anticoagulant with potent and selective factor Xa (FXa) inhibitory activity, a new series of cinnamyl derivatives with enhanced lipophilicity and prodrug forms were synthesized and their biological activities were evaluate

BENZAMIDINE DERIVATIVE

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Page 152, (2010/02/05)

Compounds of general formula (1) and pharmacologically acceptable salts thereof: ???[wherein ??????R1 represents a hydrogen atom, a halogen atom, an alkyl group or a hydroxyl group; ??????R2 represents a hydrogen atom or a halogen atom; ??????R3 represents a hydrogen atom, an alkyl group which may be substituted, an aralkyl group, an alkylcarbonyl group which may be substituted, an alkylsulfonyl group which may be substituted or the like; ??????each of R4 and R5 represents a hydrogen atom, a halogen atom, an alkyl group which may be substituted, a carbamoyl group or the like; ??????R6 represents a heterocycle or the like; ??????each of R7 and R8 represents a hydrogen atom, an alkyl group or the like; ??????n represents 0, 1 or 2] ???exhibit excellent activated blood coagulation factor X inhibitory activity and are useful for the prevention or treatment of blood coagulation-related diseases.

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