Welcome to LookChem.com Sign In|Join Free
  • or
1,2-di(2-naphthyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1332869-80-3

Post Buying Request

1332869-80-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1332869-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332869-80-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,8,6 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1332869-80:
(9*1)+(8*3)+(7*3)+(6*2)+(5*8)+(4*6)+(3*9)+(2*8)+(1*0)=173
173 % 10 = 3
So 1332869-80-3 is a valid CAS Registry Number.

1332869-80-3Relevant academic research and scientific papers

Oxidative Intramolecular C-C Bond Formation Reactions of 1,2-Diarylbenzenes: Syntheses of Highly Conjugated Double-Bridged Polycyclic Aromatic Hydrocarbons

Hirabayashi, Kazunori,Islam, Md. Rafikul,Nishinaga, Tohru,Shimizu, Toshio,Sugiura, Ken-Ichi

, (2021/10/05)

Oxidation reactions of 1,2-diarylbenzenes induce intramolecular C-C bond formation. The substrates studied were prepared by the stepwise Suzuki-Miyaura coupling reaction that introduced 2-naphthyl, 2-anthranyl, and 2-pyrenyl groups on the ortho -positions

Selective Mechanochemical Monoarylation of Unbiased Dibromoarenes by in Situ Crystallization

Seo, Tamae,Kubota, Koji,Ito, Hajime

supporting information, p. 9884 - 9889 (2020/05/19)

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of liquid, unbiased dibromoarenes under mechanochemical conditions selectively afford the monoarylated products. The lower reactivity of the crystalline monoarylated products relative to the liquid starting materials should be attributed predominantly to the low diffusion efficiency of the former in the reaction mixture, which results in a selective monoarylation. The present study sheds light on a novel approach using in situ phase transitions in solids to design selective organic transformations that are difficult to achieve via conventional solution-based synthesis.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1332869-80-3