Welcome to LookChem.com Sign In|Join Free
  • or
Benzeneacetic acid, 3-chloro-α-formyl-, ethyl ester is a chemical compound with the molecular formula C10H11ClO2. It is an ethyl ester derivative of 3-chloro-α-formylbenzeneacetic acid, characterized by its colorless liquid appearance and strong, sweet odor. Classified as a hazardous chemical, it requires careful handling and storage to prevent exposure and environmental contamination.

200215-46-9

Post Buying Request

200215-46-9 Suppliers

Recommended suppliers

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

200215-46-9 Usage

Uses

Used in Pharmaceutical Industry:
Benzeneacetic acid, 3-chloro-α-formyl-, ethyl ester is utilized as an intermediate in the synthesis of various pharmaceutical products. Its unique chemical structure contributes to the development of medications with specific therapeutic properties, making it a valuable component in drug discovery and production processes.

Check Digit Verification of cas no

The CAS Registry Mumber 200215-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,2,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 200215-46:
(8*2)+(7*0)+(6*0)+(5*2)+(4*1)+(3*5)+(2*4)+(1*6)=59
59 % 10 = 9
So 200215-46-9 is a valid CAS Registry Number.

200215-46-9Relevant academic research and scientific papers

Lewis base catalyzed asymmetric hydrosilylation of α-substituted β-enamino esters: Facile access to enantioenriched β2-amino esters via dynamic kinetic resolution

Shu, Chang,Hu, Xiao-Yan,Li, Shuai-Shuai,Yuan, Wei-Cheng,Zhang, Xiao-Mei

supporting information, p. 1879 - 1882 (2014/08/18)

A chiral Lewis base organocatalyzed asymmetric hydrosilylation of α-substituted β-enamino esters is presented. The reactions proceeded through dynamic kinetic resolution to afford various enantioenriched β2-amino esters with high yields (up to

Discovery of isoxazolinone antibacterial agents. Nitrogen as a replacement for the stereogenic center found in oxazolidinone antibacterials

Snyder, Lawrence B.,Meng, Zhaoxing,Mate, Robert,D'Andrea, Stanley V.,Marinier, Anne,Quesnelle, Claude A.,Gill, Patrice,Den Bleyker, Kenneth L.,Fung-Tomc, Joan C.,Frosco, MaryBeth,Martel, Alain,Barrett, John F.,Bronson, Joanne J.

, p. 4735 - 4739 (2007/10/03)

A series of potential antimicrobial derivatives possessing bioisosteric replacements for the central oxazolidinone ring found in oxazolidinone antibacterials have been prepared. The design concept involved replacement of the requisite sp3-hybridized stereogenic center found at the 5-position of the oxazolidinone with a nitrogen atom. The synthesis and antibacterial activity of three such ring systems, the benzisoxazolinones, pyrroles, and isoxazolinones is described.

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 200215-46-9