3880-88-4 Usage
Uses
Used in Academic and Industrial Research:
5-Methoxy-1,2,3,4-Tetrahydro-naphthalen-2-ylamine Hydrochloride is used as a research chemical for its potential role as a precursor or intermediate in the synthesis of other chemical compounds. Its application in research is driven by the need to explore its chemical properties and possible uses in various chemical reactions and processes.
Used in Chemical Synthesis:
In the field of chemical synthesis, 5-Methoxy-1,2,3,4-Tetrahydro-naphthalen-2-ylamine Hydrochloride is used as a starting material or intermediate. Its utility in this context stems from its ability to participate in various chemical reactions that can lead to the formation of new compounds with different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3880-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3880-88:
(6*3)+(5*8)+(4*8)+(3*0)+(2*8)+(1*8)=114
114 % 10 = 4
So 3880-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO.ClH/c1-13-11-4-2-3-8-7-9(12)5-6-10(8)11;/h2-4,9H,5-7,12H2,1H3;1H
3880-88-4Relevant academic research and scientific papers
Alternative and straightforward synthesis of dopaminergic 5-methoxy-1,2,3,4-tetrahydronaphthalen-2-amine
Oeztaskin, Necla,Goeksu, Sueleyman,Hasan Secen
, p. 2017 - 2024 (2011/06/24)
5-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine was synthesized from 2-naphthoic acid in six steps with an overall yield of 27%. Following the reaction sequence, bromination, esterification, substitution with NaOMe in the presence of CuI, the Birch reducti
Substituted amino-5,6,7,8-tetrahydronaphthyl-oxyacetic acids, processes for their preparation and their use as medicaments
-
, (2008/06/13)
Antithrombotic, antiatherosclerotic and antiischaemic compounds of the formula STR1 in which R1 is STR2 or SO2 R4, R3 is aryl, substituted aryl, heteroaryl, aralkyl or the group STR3 R4 is aryl or sub
α-Adrenergic Agents. 2. Synthesis and α1-Agonist Activity of 2-Aminotetralins
DeMarinis, R. M.,Shah, D. H.,Hall, R. F.,Hieble, J. P.,Pendleton, R. G.
, p. 136 - 141 (2007/10/02)
Substituted 2-aminotetralins are potent, selective, direct-acting agonists as postjunctional α1 receptors.Within this series, substituent alterations on the ring, as well as on the nitrogen, change the potency of compounds by over three orders
