3880-88-4 Usage
General Description
5-Methoxy-1,2,3,4-Tetrahydro-naphthalen-2-ylamine Hydrochloride, also known as O-4310, is an organic compound classified as an organic amine and naphthalene derivative. It is a crystalline solid with a molecular formula of C12H18NO?HCl. Specific details, such as its molecular weight, melting point, boiling point, and density, are not well-established due to its relative obscurity. It is typically used in academic or industrial research settings, where it might serve as a precursor or intermediate in the synthesis of other chemical compounds. Its toxicity and environmental impact are largely unknown and require further research. As with all chemicals, it should be handled with appropriate safety precautions.
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 articles and documents
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
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
