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1069137-53-6

N-(4-bromophenyl)-N-o-tolylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1069137-53-6 Structure

  • Basic information

    1. Product Name: N-(4-bromophenyl)-N-o-tolylacetamide
    2. Synonyms: N-(4-bromophenyl)-N-o-tolylacetamide
    3. CAS NO:1069137-53-6
    4. Molecular Formula:
    5. Molecular Weight: 304.186
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1069137-53-6.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-(4-bromophenyl)-N-o-tolylacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-bromophenyl)-N-o-tolylacetamide(1069137-53-6)
    11. EPA Substance Registry System: N-(4-bromophenyl)-N-o-tolylacetamide(1069137-53-6)

  • 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: 1069137-53-6(Hazardous Substances Data)

1069137-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1069137-53-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,9,1,3 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1069137-53:
(9*1)+(8*0)+(7*6)+(6*9)+(5*1)+(4*3)+(3*7)+(2*5)+(1*3)=156
156 % 10 = 6
So 1069137-53-6 is a valid CAS Registry Number.

1069137-53-6Relevant articles and documents

CARBAZOLE AND CARBOLINE DERIVATIVES, AND PREPARATION AND THERAPEUTIC APPLICATIONS THEREOF

-

Page/Page column 57, (2012/05/20)

Compounds of general formula (I), wherein A, Y, R1 and R2 are defined herein are useful in the treatment or prevention of proliferative diseases including cancer or infectious or parasitic diseases.

Aryl halide tolerated electrophilic amination of arylboronic acids with N-chloroamides catalyzed by CuCl at room temperature

He, Chuan,Chen, Chong,Cheng, Jin,Liu, Chao,Liu, Wei,Li, Qiang,Lei, Aiwen

supporting information; experimental part, p. 6414 - 6417 (2009/03/11)

(Chemical Equation Presented) N-Cl is no competition: Aryl halides were tolerated in an efficient ligandless CuCl-catalyzed electrophilic amination reaction of arylboronic acids with N-chloroamides (see scheme; Ac=acetoxy). This coupling proceeded smoothly at ambient temperature, and products were obtained with good to excellent yields.

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