113975-38-5 Usage
Molecular structure
A unique structure consisting of a pyridine ring fused to a pyrrole ring.
Derivative of pyrrolopyridine
It belongs to a class of compounds known as pyrrolopyridine derivatives.
Potential pharmaceutical applications
These compounds may have potential use in medicinal chemistry and drug design.
Methyl groups
Two methyl groups are attached to the nitrogen atoms in the pyrrole ring.
Interesting structural features
The compound has a distinct structure that may contribute to its potential biological activities.
Potential biological activities
The compound may exhibit biological activities that could be useful in drug design and medicinal chemistry.
Further research needed
More studies and research are required to fully understand the properties and potential applications of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 113975-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,9,7 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113975-38:
(8*1)+(7*1)+(6*3)+(5*9)+(4*7)+(3*5)+(2*3)+(1*8)=135
135 % 10 = 5
So 113975-38-5 is a valid CAS Registry Number.
113975-38-5Relevant articles and documents
Asymmetric Hydrogenation of Azaindoles: Chemo- and Enantioselective Reduction of Fused Aromatic Ring Systems Consisting of Two Heteroarenes
Makida, Yusuke,Saita, Masahiro,Kuramoto, Takahiro,Ishizuka, Kentaro,Kuwano, Ryoichi
supporting information, p. 11859 - 11862 (2016/11/16)
High enantioselectivity was achieved for the hydrogenation of azaindoles by using the chiral catalyst, which was prepared from [Ru(η3-methallyl)2(cod)] and a trans-chelating bis(phosphine) ligand (PhTRAP). The dearomative reaction exclusively occurred on the five-membered ring, thus giving the corresponding azaindolines with up to 97:3 enantiomer ratio.
Synthesis of aromatic ring fused pyrrole derivatives by palladium-catalyzed annulation of o-iodoarylamines with allyl acetate
Hong, Chang Sung,Seo, Jae Yong,Yum, Eul Kgun,Sung, Nack-Do
, p. 631 - 639 (2007/10/03)
Indoles, azaindoles, and pyrroloquinolines were obtained by palladium-catalyzed annulation of o-iodoarylamines with allyl acetate under 5 mol percent Pd(OAc)2, 1 equiv. LiCl, 3 equiv. K2CO3, and 2 equiv. allyl acetate in DMF at 120°C.
