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181473-71-2

N-(5-chloro-2-methoxybenzyl)-N-(4-methoxyphenyl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 181473-71-2 Structure

  • Basic information

    1. Product Name: N-(5-chloro-2-methoxybenzyl)-N-(4-methoxyphenyl)amine
    2. Synonyms: N-(5-chloro-2-methoxybenzyl)-N-(4-methoxyphenyl)amine
    3. CAS NO:181473-71-2
    4. Molecular Formula: C15H16ClNO2
    5. Molecular Weight: 277.74604
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 181473-71-2.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-(5-chloro-2-methoxybenzyl)-N-(4-methoxyphenyl)amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(5-chloro-2-methoxybenzyl)-N-(4-methoxyphenyl)amine(181473-71-2)
    11. EPA Substance Registry System: N-(5-chloro-2-methoxybenzyl)-N-(4-methoxyphenyl)amine(181473-71-2)

  • 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: 181473-71-2(Hazardous Substances Data)

181473-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181473-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,4,7 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 181473-71:
(8*1)+(7*8)+(6*1)+(5*4)+(4*7)+(3*3)+(2*7)+(1*1)=142
142 % 10 = 2
So 181473-71-2 is a valid CAS Registry Number.

181473-71-2Downstream Products

181473-71-2Relevant articles and documents

N-Benzylated benzimidazol-2-one derivatives: Activators of large-conductance Ca2+-dependent K+ channels

Meanwell, Nicholas A.,Sit, Sing-Yuen,Gao, Jinnian,Boissard, Christopher G.,Lum-Ragan, Janet,Dworetzky, Steven I.,Gribkoff, Valentin K.

, p. 1641 - 1646 (2007/10/03)

A series of benzimidazol-2-ones structurally homologous to the known maxi-K opener NS-004 (2) were synthesized and evaluated by electrophysiological techniques as openers of the cloned maxi-K channel mSlo expressed in Xenopus laevis oocytes. The structure-activity relationships reveal tolerance in the topological relationship between the heterocycle and the phenol hydroxy and indicate the importance of an electron withdrawing substituent on the heterocycle for expression of maxi-K opening properties. The most efficacious activators of this channel were the 5-Cl derivative 4f and the 5-NO2 analogue 4i.

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