99907-80-9 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is used as a potential pharmaceutical agent for its potential biological activity. The presence of various functional groups allows for the compound to interact with biological targets, making it a candidate for drug development, particularly in the areas of medicinal chemistry and drug discovery.
Used in Agrochemical Industry:
In the agrochemical industry, Methyl 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate may be utilized as a precursor or intermediate in the synthesis of agrochemicals, such as pesticides or herbicides. Its complex structure and functional groups could contribute to the development of novel and effective agrochemical products.
Used in Chemical Research and Development:
Methyl 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is used as a subject of research for its potential chemical properties. Methyl 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate's unique structure may lead to the discovery of new reactions or mechanisms, contributing to the advancement of organic chemistry and related fields.
Used in Material Science:
Methyl 2-amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate may also find applications in material science, where its specific molecular structure could be leveraged to develop new materials with unique properties, such as in the creation of polymers, coatings, or other advanced materials with tailored characteristics for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 99907-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,0 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99907-80:
(7*9)+(6*9)+(5*9)+(4*0)+(3*7)+(2*8)+(1*0)=199
199 % 10 = 9
So 99907-80-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO4/c1-17-11-4-5-12(18-2)10-8-14(15,13(16)19-3)7-6-9(10)11/h4-5H,6-8,15H2,1-3H3
99907-80-9Relevant academic research and scientific papers
Stereospecific Total Synthesis of 9-Aminoanthracyclines: (+)-9-Amino-9-deoxydaunomycin and Related Compounds
Ishizumi, Kikuo,Ohashi, Naohito,Tanno, Norihiko
, p. 4477 - 4485 (2007/10/02)
9-amino-9-deoxydaunomycin and related compounds, in which the hydroxyl group at the 9-position of daunomycin is replaced by an amino group, have been synthesized.Asymmetry was introduced into the synthetic sequence for the AB synthon by resolution of the intermediate amino ester or acetamido acid to afford (R)-(-)-2-acetyl-2-acetamido-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene, which was converted to the tetracyclic amido ketones by Friedel-Crafts acylation with phthalic anhydride or its 3-methoxy derivative.The resulting regioisomers 4- and 1-methoxy compounds were separed, after methylation and selective demethylation, by crystallization and preparative TLC.The required introduction of the C7-hydroxyl function proceeded stereosepcifically via a three-step reaction sequence involving formation of an oxazine compound.The silver trifluoromethane assisted glycosidation of the resulting aglycons with 2-deoxy-3,4-di-O-acetyl-D-erythro-pentopyranosyl bromide or N,O-bis(trifluoroacetyl)daunosaminyl chloride, followed by alkaline hydrolysis afforded the target glycosides.The work reported herein comprises an efficient, practical synthesis of 9-amino-9-deoxydaunomycin and its analogues with the same stereochemistry as in the naturally occurring anthracyclines.
