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methyl N-<3,5-dimethyl-4-(4'-methoxy-3'-isopropylphenoxy)phenyl>oxamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156740-80-6 Structure
  • Basic information

    1. Product Name: methyl N-<3,5-dimethyl-4-(4'-methoxy-3'-isopropylphenoxy)phenyl>oxamate
    2. Synonyms: methyl N-<3,5-dimethyl-4-(4'-methoxy-3'-isopropylphenoxy)phenyl>oxamate
    3. CAS NO:156740-80-6
    4. Molecular Formula:
    5. Molecular Weight: 371.433
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156740-80-6.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: methyl N-<3,5-dimethyl-4-(4'-methoxy-3'-isopropylphenoxy)phenyl>oxamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl N-<3,5-dimethyl-4-(4'-methoxy-3'-isopropylphenoxy)phenyl>oxamate(156740-80-6)
    11. EPA Substance Registry System: methyl N-<3,5-dimethyl-4-(4'-methoxy-3'-isopropylphenoxy)phenyl>oxamate(156740-80-6)
  • 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: 156740-80-6(Hazardous Substances Data)

156740-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156740-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,4 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156740-80:
(8*1)+(7*5)+(6*6)+(5*7)+(4*4)+(3*0)+(2*8)+(1*0)=146
146 % 10 = 6
So 156740-80-6 is a valid CAS Registry Number.

156740-80-6Relevant articles and documents

Method of treating hair loss using diphenylether derivatives

-

, (2008/06/13)

The present invention describes methods for treating hair loss in mammals, including arresting and/or reversing hair loss and promoting hair growth. The methods comprise administering a cardiac-sparing compound which is a derivative of diphenylether and p

Synthesis and Structure-Activity Relationships of Oxamic Acid and Acetic Acid Derivatives Related to L-Thyronine

Yokoyama, Naokata,Walker, Gordon N.,Main, Alan J.,Stanton, James L.,Morrissey, Michael M.,et al.

, p. 695 - 707 (2007/10/02)

Aryloxamic acids 7 and 23, (arylamino)acetic acids 29, arylpropionic acids 33, arylthioacetic acids 37, and (aryloxy)acetic acid 41 related to L-triiodothyronine (L-T3) were prepared and tested in vitro for binding to the rat liver nuclear L-T

Heteroacetic acid derivatives

-

, (2008/06/13)

Disclosed are compounds of formula STR1 wherein R is hydroxy, esterified hydroxy or etherified hydroxy; R1 is halogen, trifluoromethyl or lower alkyl; R2 is halogen, trifluoromethyl or lower alkyl; R3 is halogen, trifluoromethyl, lower alkyl, aryl, aryl-lower alkyl, cycloalkyl or cycloalkyl-lower alkyl; or R3 is the radical STR2 wherein R8 is hydrogen, lower alkyl, aryl, cycloalkyl, aryl-lower alkyl or cycloalkyl-lower alkyl; R9 is hydroxy or acyloxy; R10 represents hydrogen or lower alkyl; or R9 and R10 together represent oxo; R4 is hydrogen, halogen, trifluoromethyl or lower alkyl; X is --NR7, S or O; W is O or S; R5 represents hydrogen, lower alkyl or aryl-lower alkyl;and R6 represents hydrogen; or R5 and R6 together represent oxo provided that X represents --NR7; R7 represents hydrogen or lower alkyl; Z represents carboxyl, carboxyl derivatized as a pharmaceutically acceptable ester or as a pharmaceutically acceptable amide; and pharmaceutically acceptable salts thereof; which are useful as hypocholesteremic agents.

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