39830-66-5 Usage
Chemical Properties
off-white to green crystalline powder
Uses
Different sources of media describe the Uses of 39830-66-5 differently. You can refer to the following data:
1. ? ;Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1? ;Reactant for preparation of cytotoxic agents against multidrug-resistant cancer cells2? ;Reactant for preparation of inhibitor for β-tryptase3? ;Reactant for preparation of histamine H3 antagonists4? ;Reactant for preparation of JNK3 MAP kinase inhibitors5? ;Reactant for preparation of nucleosides6
2. Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulatorsReactant for preparation of cytotoxic agents against multidrug-resistant cancer cellsReactant for preparation of inhibitor for β-tryptaseReactant for preparation of histamine H3 antagonistsReactant for preparation of JNK3 MAP kinase inhibitorsReactant for preparation of nucleosides
Synthesis Reference(s)
Journal of Heterocyclic Chemistry, 26, p. 1405, 1989 DOI: 10.1002/jhet.5570260533Chemical and Pharmaceutical Bulletin, 29, p. 249, 1981 DOI: 10.1248/cpb.29.249
General Description
The IR and UV spectra of methyl indole-4-carboxylate was studied.
Check Digit Verification of cas no
The CAS Registry Mumber 39830-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,3 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39830-66:
(7*3)+(6*9)+(5*8)+(4*3)+(3*0)+(2*6)+(1*6)=145
145 % 10 = 5
So 39830-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c1-13-10(12)8-3-2-4-9-7(8)5-6-11-9/h2-6,11H,1H3
39830-66-5Relevant articles and documents
Synthesis of diverse indole libraries on polystyrene resin - Scope and limitations of an organometallic reaction on solid supports
Knepper, Kerstin,Vanderheiden, Sylvia,Braese, Stefan
experimental part, p. 1191 - 1199 (2012/09/07)
The synthesis of diverse substituted indole structures on solid supports is described. The immobilization of nitrobenzoic acid onto Merrifield resin and the subsequent treatment with alkenyl Grignard reagents delivered indole carboxylates bound to solid s
