Welcome to LookChem.com Sign In|Join Free

CAS

  • or
C16H15BrN2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1034257-07-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1034257-07-2 Structure
  • Basic information

    1. Product Name: C16H15BrN2O
    2. Synonyms: C16H15BrN2O
    3. CAS NO:1034257-07-2
    4. Molecular Formula:
    5. Molecular Weight: 331.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1034257-07-2.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: C16H15BrN2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H15BrN2O(1034257-07-2)
    11. EPA Substance Registry System: C16H15BrN2O(1034257-07-2)
  • 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: 1034257-07-2(Hazardous Substances Data)

1034257-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034257-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,2,5 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1034257-07:
(9*1)+(8*0)+(7*3)+(6*4)+(5*2)+(4*5)+(3*7)+(2*0)+(1*7)=112
112 % 10 = 2
So 1034257-07-2 is a valid CAS Registry Number.

1034257-07-2Downstream Products

1034257-07-2Relevant articles and documents

Light-Driven Intramolecular C?N Cross-Coupling via a Long-Lived Photoactive Photoisomer Complex

Jing, Dong,Lu, Cong,Chen, Zhuo,Jin, Songyang,Xie, Lijuan,Meng, Ziyi,Su, Zhishan,Zheng, Ke

, p. 14666 - 14672 (2019)

Reported herein is a visible-light-driven intramolecular C?N cross-coupling reaction under mild reaction conditions (metal- and photocatalyst-free, at room temperature) via a long-lived photoactive photoisomer complex. This strategy was used to rapidly prepare the N-substituted polycyclic quinazolinone derivatives with a broad substrate scope (>50 examples) and further exploited to synthesize the natural products tryptanthrin, rutaecarpine, and their analogues. The success of gram-scale synthesis and solar-driven transformation, as well as promising tumor-suppressing biological activity, proves the potential of this strategy for practical applications. Mechanistic investigations, including control experiments, DFT calculations, UV-vis spectroscopy, EPR, and X-ray single-crystal structure of the key intermediate, provides insight into the mechanism.

Metal-Free Synthesis of Polycyclic Quinazolinones Enabled by a (NH4)2S2O8-Promoted Intramolecular Oxidative Cyclization

Xie, Lijuan,Lu, Cong,Jing, Dong,Ou, Xinrui,Zheng, Ke

supporting information, p. 3649 - 3653 (2019/06/04)

An efficient metal-free, (NH4)2S2O8 mediated intramolecular oxidative cyclization for the construction of polycyclic heterocycles was disclosed. A series of polycyclic quinazolinone derivatives with good functional group tolerance were obtained in high yields. The natural products tryptanthrin and rutaecarpine, as well as their derivatives, were easily synthesized by this strategy. A preliminary mechanism study suggested the carbon-centered radical was involved in the catalytic cycle.

Fragment-based discovery of hepatitis C virus NS5b RNA polymerase inhibitors

Antonysamy, Stephen S.,Aubol, Brandon,Blaney, Jeff,Browner, Michelle F.,Giannetti, Anthony M.,Harris, Seth F.,Hebert, Normand,Hendle, Joerg,Hopkins, Stephanie,Jefferson, Elizabeth,Kissinger, Charles,Leveque, Vincent,Marciano, David,McGee, Ethel,Najera, Isabel,Nolan, Brian,Tomimoto, Masaki,Torres, Eduardo,Wright, Tobi

, p. 2990 - 2995 (2008/12/23)

Non-nucleoside inhibitors of HCV NS5b RNA polymerase were discovered by a fragment-based lead discovery approach, beginning with crystallographic fragment screening. The NS5b binding affinity and biochemical activity of fragment hits and inhibitors was de

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1034257-07-2