40302-35-0 Usage
General Description
2-(1H-Indol-3-ylmethylene)-5,5-dimethyl-1,3-cyclohexanedione is a chemical compound with a complex structure that consists of a cyclohexanedione core linked to an indole ring. 2-(1H-INDOL-3-YLMETHYLENE)-5,5-DIMETHYL-1,3-CYCLOHEXANEDIONE is a derivative of the indole family of chemicals, and it features a dimethyl substituent on the cyclohexanedione ring. The presence of the indole group in this compound suggests potential pharmacological and biological activities, as indole derivatives are known for their diverse range of biological and therapeutic properties. The precise uses and applications of 2-(1H-Indol-3-ylmethylene)-5,5-dimethyl-1,3-cyclohexanedione are not readily available, and further research may be needed to fully understand its properties and potential uses in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 40302-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,0 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40302-35:
(7*4)+(6*0)+(5*3)+(4*0)+(3*2)+(2*3)+(1*5)=60
60 % 10 = 0
So 40302-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H17NO2/c1-17(2)8-15(19)13(16(20)9-17)7-11-10-18-14-6-4-3-5-12(11)14/h3-7,10,18H,8-9H2,1-2H3
40302-35-0Relevant articles and documents
Novel, recyclable, and thermally stable task-specific ionic liquid (TBA acetate) medium/catalyst for the synthesis of indolylidinecyclic-1,3- and -1,4-diketones
Riyaz, Sd.,Indrasena,Naidu,Dubey
, p. 368 - 373 (2014/01/06)
A simple and efficient synthesis of indolylidinethiazolidnediones (3) and indolylidinecyclic-1,3-diketones (5) has been developed by reaction of indole-3-aldehyde (1) with thiazolidinedione (2) or cyclic-1,3-diketones (4) using tetra butyl ammonium acetat
