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1036334-33-4

C15H17ClN2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036334-33-4 Structure

  • Basic information

    1. Product Name: C15H17ClN2O2
    2. Synonyms:
    3. CAS NO:1036334-33-4
    4. Molecular Formula:
    5. Molecular Weight: 292.765
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036334-33-4.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: C15H17ClN2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H17ClN2O2(1036334-33-4)
    11. EPA Substance Registry System: C15H17ClN2O2(1036334-33-4)

  • 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: 1036334-33-4(Hazardous Substances Data)

1036334-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036334-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,3,3 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1036334-33:
(9*1)+(8*0)+(7*3)+(6*6)+(5*3)+(4*3)+(3*4)+(2*3)+(1*3)=114
114 % 10 = 4
So 1036334-33-4 is a valid CAS Registry Number.

1036334-33-4Downstream Products

1036334-33-4Relevant articles and documents

Pyridyl-phenyl ether monoamine reuptake inhibitors: Impact of lipophilicity on dual SNRI pharmacology and off-target promiscuity

Whitlock, Gavin A.,Fish, Paul V.,Fray, M. Jonathan,Stobie, Alan,Wakenhut, Florian

, p. 2896 - 2899 (2008/12/22)

A novel series of pyridyl-phenyl ethers are disclosed, which possess dual 5-HT and NA reuptake pharmacology with good selectivity over dopamine reuptake inhibition. An analysis of the relationship between lipophilicity and pharmacology highlighted that potent dual SNRI activity was only achievable at c log P > 3.5. The series was found to possess significant polypharmacology issues, and we concluded that this off-target promiscuity was related to lipophilicity.

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