Welcome to LookChem.com Sign In|Join Free
  • or
2-(methyl-phenyl-amino)-propionic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

214709-69-0

Post Buying Request

214709-69-0 Suppliers

Recommended suppliers

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

214709-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214709-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,7,0 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 214709-69:
(8*2)+(7*1)+(6*4)+(5*7)+(4*0)+(3*9)+(2*6)+(1*9)=130
130 % 10 = 0
So 214709-69-0 is a valid CAS Registry Number.

214709-69-0Downstream Products

214709-69-0Relevant academic research and scientific papers

Directed Evolution of Artificial Metalloenzymes in Whole Cells

Bloomer, Brandon J.,Chen, Reichi,Clark, Douglas S.,Gu, Yang,Hartwig, John F.,Liu, Zhennan

supporting information, (2021/12/24)

Artificial metalloenzymes (ArMs), created by introducing synthetic cofactors into protein scaffolds, are an emerging class of catalyst for non-natural reactions. Although many classes of ArMs are known, in vitro reconstitution of cofactors and proteins ha

Asymmetric N-H Insertion of secondary and primary anilines under the catalysis of palladium and chiral guanidine derivatives

Zhu, Yin,Liu, Xiaohua,Dong, Shunxi,Zhou, Yuhang,Li, Wei,Lin, Lili,Feng, Xiaoming

, p. 1636 - 1640 (2014/03/21)

Efficient enantioselective N-H insertion reactions of secondary and primary anilines were catalyzed by palladium(0) in combination with chiral guanidine derivatives. A broad range of substituted anilines were tolerated, and the corresponding products were obtained in high yield (up to 99 %) with good enantioselectivity (up to 94 % ee) under mild reaction conditions. The N-H insertion mechanism was examined by the study of kinetic isotope effects, control experiments, HRMS, and spectroscopic analysis. Hidden talents: Chiral guanidine derivatives were developed as useful ligands for the enantioselective insertion of carbenoids into the N-H bonds of secondary and primary anilines in combination with palladium(0), which was not previously known to promote asymmetric N-H insertion (see scheme; dba=dibenzylideneacetone). The N-H insertion mechanism was examined by kinetic isotope studies, control experiments, HRMS, and spectroscopic analysis. Copyright

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 214709-69-0