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177587-71-2

(+/-)-3-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-pentylpropionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 177587-71-2 Structure

  • Basic information

    1. Product Name: (+/-)-3-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-pentylpropionic acid
    2. Synonyms: (+/-)-3-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-pentylpropionic acid
    3. CAS NO:177587-71-2
    4. Molecular Formula:
    5. Molecular Weight: 370.489
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177587-71-2.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-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-pentylpropionic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-3-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-pentylpropionic acid(177587-71-2)
    11. EPA Substance Registry System: (+/-)-3-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-pentylpropionic acid(177587-71-2)

  • 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: 177587-71-2(Hazardous Substances Data)

177587-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177587-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,8 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 177587-71:
(8*1)+(7*7)+(6*7)+(5*5)+(4*8)+(3*7)+(2*7)+(1*1)=192
192 % 10 = 2
So 177587-71-2 is a valid CAS Registry Number.

177587-71-2Relevant articles and documents

Synthesis and SAR of 1-alkyl-2-phenylethylamine derivatives designed from N,N-dipropyl-4-methoxy-3-(2-phenylethoxy)phenylethylamine to discover σ1 ligands

Nakazato, Atsuro,Kumagai, Toshihito,Ohta, Kohmei,Chaki, Shigeyuki,Okuyama, Shigeru,Tomisawa, Kazuyuki

, p. 3965 - 3970 (2007/10/03)

The synthesis and structure-activity relationships (SAR) of 1-alkyl-2- phenylethylamine derivatives 5-8 designed from N,N-dipropyl-2-[4-methoxy-3- (2-phenylethoxy)phenyl]ethylamine hydrochloride (1, NE-100) are presented. The SAR between compound 1 and 1-alkyl-2-phenylethylamine derivatives suggested that the alkyl group on the 1-position carbon of 2-[4-methoxy-3-(2- phenylethyl)phenyl]ethylamine derivatives played the role of one of the propyl groups on the aminic nitrogen of compound 1. (-)-N-Propyl-1-butyl-2- [4-methoxy-3-(2-phenylethoxy)phenyl]ethylamine hydrochloride ((-)-6d, NE-537) and (-)-N-propyl-1-(3-methybutyl)-2-[4-methoxy-3-(2- phenylethoxy)phenyl]ethylamine hydrochloride ((-)-6i, NE-535), typical compounds in this series, have potent and selective σ1 affinity.

Optically active substituted phenylalkylamine derivatives

-

, (2008/06/13)

The present invention relates to an optically active, substituted phenylalkylamine derivative represented by Formula [1]: STR1 wherein A is a substituted or non-substituted phenyl or thienyl; X1 is hydrogen, halogen, hydroxyl or a substituted o

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