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885673-11-0

N-[1-(4-chloro-phenyl)-3-dimethylamino-propyl]-2-methoxy-2-phenyl-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • N-[1-(4-chloro-phenyl)-3-dimethylamino-propyl]-2-methoxy-2-phenyl-acetamide

    Cas No: 885673-11-0

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  • 885673-11-0 Structure

  • Basic information

    1. Product Name: N-[1-(4-chloro-phenyl)-3-dimethylamino-propyl]-2-methoxy-2-phenyl-acetamide
    2. Synonyms:
    3. CAS NO:885673-11-0
    4. Molecular Formula:
    5. Molecular Weight: 360.884
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885673-11-0.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: N-[1-(4-chloro-phenyl)-3-dimethylamino-propyl]-2-methoxy-2-phenyl-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[1-(4-chloro-phenyl)-3-dimethylamino-propyl]-2-methoxy-2-phenyl-acetamide(885673-11-0)
    11. EPA Substance Registry System: N-[1-(4-chloro-phenyl)-3-dimethylamino-propyl]-2-methoxy-2-phenyl-acetamide(885673-11-0)

  • 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: 885673-11-0(Hazardous Substances Data)

885673-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 885673-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,6,7 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 885673-11:
(8*8)+(7*8)+(6*5)+(5*6)+(4*7)+(3*3)+(2*1)+(1*1)=220
220 % 10 = 0
So 885673-11-0 is a valid CAS Registry Number.

885673-11-0Relevant articles and documents

Novel potent and efficacious nonpeptidic urotensin II receptor agonists

Lehmann, Fredrik,Pettersen, Anna,Currier, Erika A.,Sherbukhin, Vladimir,Olsson, Roger,Hacksell, Uli,Luthman, Kristina

, p. 2232 - 2240 (2007/10/03)

Six different series of nonpeptidic urotensin II receptor agonists have been synthesized and evaluated for their agonistic activity in a cell-based assay (R-SAT). The compounds are ring-opened analogues of the isochromanone-based agonist AC-7954 with different functionalities constituting the linker between the two aromatic ring moieties. Several of the compounds are highly potent and efficacious, with N-[1-(4-chlorophenyl)-3-(dimethylamino)- propyl]-4-phenylbenzamide oxalate (5d) being the most potent. The pure enantiomers of 5d were obtained from the corresponding diastereomeric amides. It was shown by a combination of X-ray crystallography and chemical correlation that the activity resides in the S-enantiomer of 5d (pEC50 7.49).

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