Welcome to LookChem.com Sign In|Join Free
  • or
Pyridine, 2-(3-chlorophenyl)-6-methyl, is an organic compound with the chemical formula C12H10ClN. It is a derivative of pyridine, a heterocyclic aromatic compound consisting of a six-membered ring with one nitrogen atom. This specific compound features a 3-chlorophenyl group attached to the 2-position and a methyl group at the 6-position. It is a colorless to pale yellow solid with a molecular weight of 207.67 g/mol. Pyridine, 2-(3-chlorophenyl)-6-methyl- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its potential applications and reactivity, it is essential to handle it with care, as it may have toxic or hazardous properties.

4385-66-4

Post Buying Request

4385-66-4 Suppliers

Recommended suppliers

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

4385-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4385-66-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4385-66:
(6*4)+(5*3)+(4*8)+(3*5)+(2*6)+(1*6)=104
104 % 10 = 4
So 4385-66-4 is a valid CAS Registry Number.

4385-66-4Downstream Products

4385-66-4Relevant academic research and scientific papers

Palladium-catalyzed Heck-type reaction of oximes with allylic alcohols: Synthesis of pyridines and azafluorenones

Zheng, Meifang,Chen, Pengquan,Wu, Wanqing,Jiang, Huanfeng

, p. 84 - 87 (2016)

We describe herein a palladium-catalyzed Heck-type reaction of O-acetyl ketoximes and allylic alcohols to synthesise pyridines. This protocol allows the robust synthesis of pyridines and azafluorenones in good to excellent yields with tolerance of various functional groups under mild conditions. The reaction is supposed to go through an oxidative addition of oximes to palladium(0) complexes, generating an alkylideneamino-palladium(ii) species, which is utilized as a key intermediate to capture the nonbiased alkenes for carbon-carbon bond formation.

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 4385-66-4