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390407-62-2

1-Propanol, 3-[[1,1-dimethyl-2-(phenylmethoxy)ethyl]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 390407-62-2 Structure

  • Basic information

    1. Product Name: 1-Propanol, 3-[[1,1-dimethyl-2-(phenylmethoxy)ethyl]amino]-
    2. Synonyms:
    3. CAS NO:390407-62-2
    4. Molecular Formula: C14H23NO2
    5. Molecular Weight: 237.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 390407-62-2.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: 1-Propanol, 3-[[1,1-dimethyl-2-(phenylmethoxy)ethyl]amino]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Propanol, 3-[[1,1-dimethyl-2-(phenylmethoxy)ethyl]amino]-(390407-62-2)
    11. EPA Substance Registry System: 1-Propanol, 3-[[1,1-dimethyl-2-(phenylmethoxy)ethyl]amino]-(390407-62-2)

  • 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: 390407-62-2(Hazardous Substances Data)

390407-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 390407-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,0,4,0 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 390407-62:
(8*3)+(7*9)+(6*0)+(5*4)+(4*0)+(3*7)+(2*6)+(1*2)=142
142 % 10 = 2
So 390407-62-2 is a valid CAS Registry Number.

390407-62-2Relevant articles and documents

Synthesis, in vitro metabolic studies, and antitumour activity of methyl analogues of ifosfamide

Misiura, Konrad,Kardacka, Karina,Kusnierczyk, Halina

, p. 291 - 294 (2001)

Synthesis of 2-chloro-1,1-dimethylethyl and 2-chloro-2,2-dimethylethyl analogues of ifosfamide was performed via aziridine intermediate. In vitro metabolic activation showed that both compounds are metabolised at a rate similar to the parent drug. However, their anticancer activity against L1210 leukaemia in mice was lower as compared with ifosfamide. The reduction of antitumour efficiency of examined analogues is probably caused by a lower ability to cross-link DNA by their final, active metabolites.

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