139167-47-8 Usage
Chemical category
Imidazolium salts
Molecular structure
Complex, with multiple functional groups
Functional groups
Ethyl, propenyl, and naphthyl
Potential applications
Organic synthesis, catalysis, and materials science
Structural and electronic properties
Unique, contributing to its potential applications
Biological activities
Potential, could be useful in pharmaceutical development
Diverse applications
Possible due to its unique properties and potential uses
Further study
Necessary to fully understand its properties and potential uses
Check Digit Verification of cas no
The CAS Registry Mumber 139167-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,6 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 139167-47:
(8*1)+(7*3)+(6*9)+(5*1)+(4*6)+(3*7)+(2*4)+(1*7)=148
148 % 10 = 8
So 139167-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C29H33N3.ClH/c1-6-31-25-19-21-13-8-9-14-22(21)20-26(25)32(7-2)28(31)18-12-17-27-29(3,4)23-15-10-11-16-24(23)30(27)5;/h8-20,28H,6-7H2,1-5H3;1H/b18-12+,27-17+;
139167-47-8Relevant articles and documents
Synthesis and substance P antagonist activity of naphthimidazolium derivatives
Lawrence,Venepalli,Appell,Goswami,Logan,Tomczuk,Yanni
, p. 1273 - 1279 (2007/10/02)
The synthesis of unsymmetrical naphth[2,3-d]imidazolium and bridged naphth[2,3-d]imidazolium derivatives and their substance P (SP) antagonist activity are described. All compounds were evaluated for their ability to displace SP from neurokinin-1 (NK-1) receptor sites using standard receptor binding methodology (rat forebrain membrane). 1,3-Diethyl-2-[3-(1,3-dihydro- 1,3,3-trimethyl-2H-indol-2-ylidene)-1-propenyl]-1H-naphth[2,3-d]imidazolium chloride (7a), a representative compound in this series, was further evaluated for SP antagonist activity in a guinea pig ileum contractility assay. In vivo SP antagonist activity of 7a was demonstrated using SP-induced salivation and paw edema models performed in rats.
