108439-67-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3-Ethoxy-4-methoxy-benzylamine is utilized as a building block in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its unique structure and functional groups contribute to the development of new and effective compounds in these industries.
Used in Dye and Pigment Production:
This chemical compound is also employed in the production of dyes, pigments, and other specialty chemicals, where its aromatic amine nature and functional groups enhance the color and properties of the final products.
Used in Drug Discovery and Medicinal Chemistry:
Due to its potential applications in drug discovery and medicinal chemistry, 3-ethoxy-4-methoxy-benzylamine is used as a key intermediate in the synthesis of novel drug candidates. Its unique structural properties and functional groups allow for the exploration of new therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 108439-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,3 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108439-67:
(8*1)+(7*0)+(6*8)+(5*4)+(4*3)+(3*9)+(2*6)+(1*7)=134
134 % 10 = 4
So 108439-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-3-13-10-6-8(7-11)4-5-9(10)12-2/h4-6H,3,7,11H2,1-2H3
108439-67-4Relevant articles and documents
5-Alkylated thiazolidinones as follicle-stimulating hormone (FSH) receptor agonists
Wrobel, Jay,Jetter, James,Kao, Wenling,Rogers, John,Di, Li,Chi, Jamin,Perez, M. Claudia,Chen, Gi-Chung,Shen, Emily S.
, p. 5729 - 5741 (2006)
We prepared analogs of potent thiazolidinone-based follicle-stimulating hormone (FSH) agonists 1, that is, 3 that contained an additional 5-alkyl substituent. This extra substituent was added to reduce synthetic problems that arose during preparation of a
PYRIDO[2,3-D]PYRIMIDINE-2,4-DIAMINES AS PDE 2 INHIBITORS
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Page/Page column 28, (2010/02/12)
The invention provides compounds of formula (I) prodrugs thereof, and the pharmaceutically acceptable salts of the compounds or prodrugs, wherein n, X, and Y are as defined herein; pharmaceutical compositions thereof; combinations thereof; and uses thereo
Anthranilic acid derivatives as inhibitors of the cGMP-phosphodiesterase
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, (2008/06/13)
Compounds of formula (I) STR1where R 1 is hydrogen; R 2 is nitro, cyano or halo(lower)alkyl; R 3 is phenyl substituted with one or more substituents selected from halogen, cyano and lower alkoxy; A is a lower alkylene group; R 4 is a group CR 6 R 7 R 8 wherein R 6 and R 7 form, together with the carbon atom to which they are attached a cycloalkyl group optionally substituted with hydroxy, lower alkoxy or a lower alkanoylamino; and R 8 is hydrogen; its prodrug and a salt thereof.