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N-methyl-N-(1-methyl-2-{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}ethyl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126002-06-0 Structure
  • Basic information

    1. Product Name: N-methyl-N-(1-methyl-2-{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}ethyl)amine
    2. Synonyms: N-methyl-N-(1-methyl-2-{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}ethyl)amine
    3. CAS NO:126002-06-0
    4. Molecular Formula: C16H26N2O
    5. Molecular Weight: 262.39044
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126002-06-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-methyl-N-(1-methyl-2-{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}ethyl)amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-N-(1-methyl-2-{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}ethyl)amine(126002-06-0)
    11. EPA Substance Registry System: N-methyl-N-(1-methyl-2-{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}ethyl)amine(126002-06-0)
  • 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: 126002-06-0(Hazardous Substances Data)

126002-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126002-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,0 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 126002-06:
(8*1)+(7*2)+(6*6)+(5*0)+(4*0)+(3*2)+(2*0)+(1*6)=70
70 % 10 = 0
So 126002-06-0 is a valid CAS Registry Number.

126002-06-0Downstream Products

126002-06-0Relevant articles and documents

POTENTIAL ANTIDEPRESSANTS: 1-(4-(AMINOALKOXY)PHENYL)-2-PROPYLAMINES

Kmonicek, Vojtech,Vejdelek, Zdenek,Holubek, Jiri,Valchar, Martin,Protiva, Miroslav

, p. 1721 - 1733 (2007/10/02)

1-(4-Hydroxyphenyl)-2-propylamine (X) and its N-monomethyl (XI) and N,N-dimethyl (XII) derivatives were O-alkylated with six tert.aminoalkyl chlorides to aminoalkyl ethers Ia-VIc.In cases of X and XI the reactions were complicated by O,N-dialkylation leading to isolation of triamino ethers XVI and XVII. 1-(4-Hydroxyphenyl)propan-2-one was alkylated with 2-dimethylaminoethyl chloride and the ether XIII was obtained.An attempt to transform 4-(2-dimethylaminoethoxy)benzaldehyde to the 1-aryl-2-nitropropene XIV by heating with nitroethane in acetic acid in the presence of ammonium acetate resulted in the formation of 4-(2-dimethylaminoethoxy)benzonitrile (XV).In the form of salts the amino ethers prepared were tested for antidepressant activity but proved little active or inactive.

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