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

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  • 135569-16-3 Structure
  • Basic information

    1. Product Name: 4-nitrocaramiphen
    2. Synonyms: 4-nitrocaramiphen;2-(diethylamino)ethyl 1-(4-nitrophenyl)cyclopentanecarboxylate
    3. CAS NO:135569-16-3
    4. Molecular Formula: C18H26N2O4
    5. Molecular Weight: 334.41004
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135569-16-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 454.5±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.150±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.24±0.25(Predicted)
    10. CAS DataBase Reference: 4-nitrocaramiphen(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-nitrocaramiphen(135569-16-3)
    12. EPA Substance Registry System: 4-nitrocaramiphen(135569-16-3)
  • 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: 135569-16-3(Hazardous Substances Data)

135569-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135569-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,6 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135569-16:
(8*1)+(7*3)+(6*5)+(5*5)+(4*6)+(3*9)+(2*1)+(1*6)=143
143 % 10 = 3
So 135569-16-3 is a valid CAS Registry Number.

135569-16-3Downstream Products

135569-16-3Relevant articles and documents

Muscarinic Receptor Binding Profile of Para-Substituted Caramiphen Analogues

Hudkins, Robert L.,DeHaven-Hudkins, Diane L.,Stubbins, James F.

, p. 2984 - 2989 (2007/10/02)

Para-substituted analogues of the antimuscarinic agent caramiphen were synthesized and evaluated for their ability to bind to the M1 and M2 subtypes of the muscarinic receptor.The purpose of the set to look for a possible relationshi

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