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CAS

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1416727-78-0

N-(1-(4-bromophenyl)-2-(4-chlorophenyl)ethyl)-4-methoxyaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1416727-78-0 Structure

  • Basic information

    1. Product Name: N-(1-(4-bromophenyl)-2-(4-chlorophenyl)ethyl)-4-methoxyaniline
    2. Synonyms:
    3. CAS NO:1416727-78-0
    4. Molecular Formula:
    5. Molecular Weight: 416.745
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1416727-78-0.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: N-(1-(4-bromophenyl)-2-(4-chlorophenyl)ethyl)-4-methoxyaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-(4-bromophenyl)-2-(4-chlorophenyl)ethyl)-4-methoxyaniline(1416727-78-0)
    11. EPA Substance Registry System: N-(1-(4-bromophenyl)-2-(4-chlorophenyl)ethyl)-4-methoxyaniline(1416727-78-0)

  • 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: 1416727-78-0(Hazardous Substances Data)

1416727-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1416727-78-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,7,2 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1416727-78:
(9*1)+(8*4)+(7*1)+(6*6)+(5*7)+(4*2)+(3*7)+(2*7)+(1*8)=170
170 % 10 = 0
So 1416727-78-0 is a valid CAS Registry Number.

1416727-78-0Downstream Products

1416727-78-0Relevant articles and documents

Highly enantioselective hydrosilylation of N-(1,2-diarylethylidene) arylamines

Zheng, Yongsheng,Xue, Zhouyang,Liu, Lixin,Shu, Chang,Yuan, Weicheng,Zhang, Xiaomei

, p. 412 - 415 (2013/02/23)

By employing a chiral Lewis base as the catalyst, enantioselective hydrosilylation of N-(1,2-diarylethylidene)arylamines was realized. The reactions proceeded smoothly to afford various chiral 1,2-diarylethanamines with good yields (up to 99%) in good ena

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