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1352004-93-3

2-methoxy-4-{[(2-piperazin-1-ylethyl)imino]methyl}phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352004-93-3 Structure

  • Basic information

    1. Product Name: 2-methoxy-4-{[(2-piperazin-1-ylethyl)imino]methyl}phenol
    2. Synonyms: 2-methoxy-4-{[(2-piperazin-1-ylethyl)imino]methyl}phenol
    3. CAS NO:1352004-93-3
    4. Molecular Formula:
    5. Molecular Weight: 263.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352004-93-3.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: 2-methoxy-4-{[(2-piperazin-1-ylethyl)imino]methyl}phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methoxy-4-{[(2-piperazin-1-ylethyl)imino]methyl}phenol(1352004-93-3)
    11. EPA Substance Registry System: 2-methoxy-4-{[(2-piperazin-1-ylethyl)imino]methyl}phenol(1352004-93-3)

  • 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: 1352004-93-3(Hazardous Substances Data)

1352004-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352004-93-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,0,0 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1352004-93:
(9*1)+(8*3)+(7*5)+(6*2)+(5*0)+(4*0)+(3*4)+(2*9)+(1*3)=113
113 % 10 = 3
So 1352004-93-3 is a valid CAS Registry Number.

1352004-93-3Relevant articles and documents

Synthesis and antimicrobial screening of 4-thiazolidinone and 2-azetidinone derivatives of piperazine

Shingade, Sunil G.,Bari, Sanjaykumar B.

, p. 699 - 706 (2013)

The Schiff's bases 3a-3h were synthesized by reacting substituted/ unsubstituted aromatic aldehydes 2a-2h with 1-(2-aminoethyl)-piperazine 1. A series of novel aryl-3-(2-piperazin-1-ylethyl)-1,3-thiazolidin-4-one 4a-4h and 3-chloro-1-{2-[4-(chloroacetyl)piperazin-1-yl]ethyl}-4-arylazetidin-2-one 5a-5h were synthesized from the Schiff's bases of 1-(2-aminoethyl)-piperazine 3a-3h. The structures of synthesized compounds were confirmed by analytical (C, H, and N) and spectral (FT-IR, 1H NMR, 13C NMR, and Mass) data. The compounds 4a-4h and 5a-5h were screened for antimicrobial activity. The compounds 4a, 4d, 4f, 4g, 5a, 5d, 5f, and 5g exhibited substantially significant antibacterial as well as antifungal activity.

Synthesis, anti-inflammatory and anticancer activity evaluation of some mono-And bis-Schiff's bases

Sondhi, Sham M.,Arya, Surbhi,Rani, Reshma,Kumar, Nikhil,Roy, Partha

, p. 3620 - 3628 (2013/02/23)

Several mono-Schiff's bases (3a-i) and bis-Schiff's bases (5a-f) were synthesized using microwave irradiation technique (3a-h, 5a-c) and by simply grinding at room temperature for a few minutes (3i, 5d-f). All these compounds were characterized by spectroscopic means and elemental analysis. They were screened for anti-inflammatory and anticancer activities (against five human cancer cell lines). Compound 5f exhibited good anti-inflammatory and compounds 3f, 5a-f exhibited good anticancer activity. Springer Science+Business Media, LLC 2011.

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