74973-30-1 Usage
Description
4,6-DIMETHOXY-3-METHYLINDOLE, 97% is an organic compound with the molecular formula C11H13NO2. It is a derivative of indole, which is a heterocyclic aromatic organic compound. 4,6-DIMETHOXY-3-METHYLINDOLE, 97% is characterized by the presence of two methoxy groups at the 4th and 6th positions, and a methyl group at the 3rd position. It is widely used in various chemical reactions and synthesis processes due to its unique structural features.
Uses
Used in Chemical Synthesis:
4,6-DIMETHOXY-3-METHYLINDOLE, 97% is used as a reactant for acid-catalyzed reactions with ketones, which are essential in the synthesis of various organic compounds. Its presence in these reactions enhances the reactivity and selectivity of the process, leading to the formation of desired products with improved yields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,6-DIMETHOXY-3-METHYLINDOLE, 97% is used as a reactant for the synthesis of pyrrolo[1,2-a]indoles. These compounds are known for their diverse biological activities, including potential applications in the treatment of various diseases. The use of this compound in the synthesis of pyrrolo[1,2-a]indoles allows for the development of novel drug candidates with improved pharmacological properties.
Used in Organic Chemistry Research:
4,6-DIMETHOXY-3-METHYLINDOLE, 97% is also used as a reactant for the synthesis of indolo[2,3-c]quinolines. These compounds are of significant interest in organic chemistry due to their unique structural features and potential applications in various fields, including material science and pharmaceuticals. The use of this compound in the synthesis of indolo[2,3-c]quinolines enables researchers to explore new avenues in chemical research and develop innovative applications.
Used in Nitration and Oxidative Dimerization Reactions:
In the field of organic chemistry, 4,6-DIMETHOXY-3-METHYLINDOLE, 97% is utilized as a reactant in nitration and oxidative dimerization reactions with nitric acid. These reactions are crucial for the functionalization of organic compounds and the formation of new chemical entities with diverse properties. The use of this compound in these reactions allows for the synthesis of a wide range of products with potential applications in various industries, such as agrochemicals, dyes, and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 74973-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74973-30:
(7*7)+(6*4)+(5*9)+(4*7)+(3*3)+(2*3)+(1*0)=161
161 % 10 = 1
So 74973-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO2/c1-7-6-12-9-4-8(13-2)5-10(14-3)11(7)9/h4-6,12H,1-3H3
74973-30-1Relevant articles and documents
Synthesis of activated 3-substituted indoles: An optimised one-pot procedure
Pchalek, Karin,Jones, Ashley W.,Wekking, Monique M.T.,Black, David StC.
, p. 77 - 82 (2007/10/03)
3-Substituted-4,6-dimethoxyindoles can be synthesised in a one-pot procedure from 3,5-dimethoxyaniline and 2-haloketones in the presence of lithium bromide and sodium bicarbonate. Graphical Abstract.
Metal Template Reactions. XX. Macrocyclic Metal Complexes Derived from 4,6-Dimethoxy-3-methylindole-2,7-dicarbaldehyde and Some Primary Diamines with Additional Nitrogen Donor Atoms
Black, David St. C.,Rothnie, Neil E.,Wong Laurence C. H.
, p. 2407 - 2412 (2007/10/02)
4,6-Dimethoxy-3-methylindole-2,7-dicarbaldehyde (6) has been prepared by the formylation of 4,6-dimethoxy-3-methylindole (5), itself prepared by the hydride reduction of the oxoindole (4).Macrocyclic nickel(II) and copper(II) complexes (8), (10) and (12) have been prepared from the dialdehyde (6), the apprppriate metal(II) acetate and the primary diamines 2,2'-iminobisaniline (7), 2-amino-N-(2'-aminophenyl)benzamide (9) and 2-amino-N-(2'-aminobenzoyl)benzamide (11) respectively.
