306935-10-4 Usage
Appearance
Yellow solid
Purity
97%
Usage
Pharmaceutical and research applications
Amino group
Provides reactivity and potential for forming bonds with other molecules
Fluorophenyl group
Adds unique properties and may influence the compound's biological activity
Thienyl group
Contributes to the compound's structure and potential applications
Development of new drugs or treatments
Due to its unique chemical structure and groups
Biological activity
May have an effect on biological systems
Precursor in organic synthesis
Can be used to create other compounds in drug discovery
Versatility
Has potential applications in various fields due to its unique properties and chemical structure
Check Digit Verification of cas no
The CAS Registry Mumber 306935-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,3 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 306935-10:
(8*3)+(7*0)+(6*6)+(5*9)+(4*3)+(3*5)+(2*1)+(1*0)=134
134 % 10 = 4
So 306935-10-4 is a valid CAS Registry Number.
306935-10-4Relevant articles and documents
2-Bromo-2-chloro-3-arylpropanenitriles as C-3 Synthons for the Synthesis of Functionalized 3-Aminothiophenes
Batsyts, Sviatoslav,Shehedyn, Maksym,Goreshnik, Evgeny A.,Obushak, Mykola D.,Schmidt, Andreas,Ostapiuk, Yurii V.
, p. 7842 - 7856 (2019)
2-Bromo-2-chloro-3-arylpropanenitriles can be prepared by Meerwein reaction from 2-chloroacrylonitrile and various aryldiazonium salts under copper(II) bromide catalysis. They proved to be stable compounds which form 2-chlorocinnnamonitriles upon treatment with bases. Reaction of the title compounds with substituted thioglycolates gave substituted 3-aminothiophenes which have not yet been accessible by other routes. Three-component reactions with the title compound, sodium sulfide and bromonitromethane, chloroacetonitrile, or ethyl 4-chloroacetoacetate gave 2-nitro- and 2-cyano-substituted 3-aminothiophenes, and thienopyridinediones in high yields and in one single step, respectively.
