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331719-47-2

N-(2-bromophenyl)-3-methylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 331719-47-2 Structure

  • Basic information

    1. Product Name: N-(2-bromophenyl)-3-methylbenzamide
    2. Synonyms: N-(2-bromophenyl)-3-methylbenzamide
    3. CAS NO:331719-47-2
    4. Molecular Formula: C14H12BrNO
    5. Molecular Weight: 290.15518
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 331719-47-2.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-(2-bromophenyl)-3-methylbenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-bromophenyl)-3-methylbenzamide(331719-47-2)
    11. EPA Substance Registry System: N-(2-bromophenyl)-3-methylbenzamide(331719-47-2)

  • 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: 331719-47-2(Hazardous Substances Data)

331719-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331719-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,7,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 331719-47:
(8*3)+(7*3)+(6*1)+(5*7)+(4*1)+(3*9)+(2*4)+(1*7)=132
132 % 10 = 2
So 331719-47-2 is a valid CAS Registry Number.

331719-47-2Downstream Products

331719-47-2Relevant articles and documents

Photocatalyst- And Transition-Metal-Free Visible-Light-Promoted Intramolecular C(sp2)-S Formation

Wang, Hao,Wu, Qi,Zhang, Jian-Dong,Li, Hai-Yan,Li, Hong-Xi

supporting information, p. 2078 - 2083 (2021/04/05)

A photocatalyst- and transition-metal-free visible-light-induced cyclization of ortho-halothiobenzanilides has been developed. Upon irradiation with visible light, substrates undergo dehalogenative cyclization to 2-aryl benzothiazoles with high efficiency and selectivity. This photocyclization exhibits a high tolerance to various functional groups, is applicable for the synthesis of 2-alkyl benzothiazoles, and is easy to set up for gram-scale reaction.

Structural development studies of anti-hepatitis C virus agents with a phenanthridinone skeleton

Nakamura, Masahiko,Aoyama, Atsushi,Salim, Mohammed T.A.,Okamoto, Mika,Baba, Masanori,Miyachi, Hiroyuki,Hashimoto, Yuichi,Aoyama, Hiroshi

scheme or table, p. 2402 - 2411 (2010/06/20)

A phenanthridinone skeleton was derived from our previous researches on thalidomide and retinoids as a multi-template for generation of anti-viral lead compounds. Structural development studies focusing on anti-hepatitis C virus activity afforded 5-butyl-2-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenanthridin-6(5H)-one (10) and 5-butylbenzo[b]phenanthridin-6(5H)-one (39), which showed EC50 values of approximately 3.7 and 3.2 μM, respectively.

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