Welcome to LookChem.com Sign In|Join Free

CAS

  • or

39077-58-2

Post Buying Request

39077-58-2 Suppliers

Recommended suppliersmore

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

39077-58-2 Usage

Also Known As

2-cyano-3-(2-pyridinyl)-2-propene

Chemical Class

Aryl nitriles

Chemical Structure

Consists of a pyridine ring attached to a propenenitrile moiety

Common Uses

Synthesis of various organic compounds
Found in pharmaceuticals, agrochemicals, and materials science

Investigated Applications

Medicinal chemistry for drug development

Potential Applications

Treatment of various diseases

Variability

Specific uses and properties may vary depending on application and formulation.

Check Digit Verification of cas no

The CAS Registry Mumber 39077-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,7 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39077-58:
(7*3)+(6*9)+(5*0)+(4*7)+(3*7)+(2*5)+(1*8)=142
142 % 10 = 2
So 39077-58-2 is a valid CAS Registry Number.

39077-58-2Downstream Products

39077-58-2Relevant articles and documents

Manganese(I)-Catalyzed H-P Bond Activation via Metal-Ligand Cooperation

Pérez, Juana M.,Postolache, Roxana,Casti?eira Reis, Marta,Sinnema, Esther G.,Vargová, Denisa,De Vries, Folkert,Otten, Edwin,Ge, Luo,Harutyunyan, Syuzanna R.

supporting information, p. 20071 - 20076 (2021/12/03)

Here we report that chiral Mn(I) complexes are capable of H-P bond activation. This activation mode enables a general method for the hydrophosphination of internal and terminal α,β-unsaturated nitriles. Metal-ligand cooperation, a strategy previously not considered for catalytic H-P bond activation, is at the base of the mechanistic action of the Mn(I)-based catalyst. Our computational studies support a stepwise mechanism for the hydrophosphination and provide insight into the origin of the enantioselectivity.

A Catalytic Peterson-like Synthesis of Alkenyl Nitriles

Lanari, Daniela,Alonzi, Matteo,Ferlin, Francesco,Santoro, Stefano,Vaccaro, Luigi

supporting information, p. 2680 - 2683 (2016/06/15)

A heterogeneous fluoride catalyst was found to enable the straightforward formation of alkenyl nitriles from the reaction of aldehydes and simple or substituted acetonitriles, in the presence of commercially available silazanes and in solvent-free conditions. The protocol afforded the products in good to excellent yields with selectivity values dependent on the nature of the substrates. It represents an alternative to classic approaches using stoichiometric strong bases, and the catalyst can be easily recovered and reused for consecutive cycles.

5, 7-SUBSTITUTED-IMIDAZO [1, 2-C] PYRIMIDINES AS INHIBITORS OF JAK KINASES

-

Page/Page column 79, (2011/11/01)

Compounds of Formula I: (Formula should be inserted here) and stereoisomers and pharmaceutically acceptable salts and solvates thereof in which R1, R2, R3, R4, R5, R6, R7, X1 and X2 have the meanings given in the specification, are inhibitors of one or more JAK kinases and are useful in the treatment of autoimmune diseases, inflammatory diseases, rejection of transplanted organs, tissues and cells, as well as hematologic disorders and malignancies and their co-morbidities.

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 39077-58-2