736173-15-2 Usage
Molecular Structure
The compound consists of a naphthalen-1-ol molecule with an attached 3-bromo-phenyl and amino group.
Functional Groups
The compound contains an amino group (-NH2) and a bromine atom (Br) attached to a phenyl group.
Salt Form
The hydrochloride salt form of the compound enhances its stability and solubility in water.
Uses
The compound is commonly used as an intermediate or building block in the synthesis of other compounds in laboratory research and pharmaceutical development.
Biological/Pharmacological Activity
The compound may have potential biological or pharmacological activity due to its structure and functional groups, making it of interest in drug discovery and medicinal chemistry.
Versatility
The compound has a variety of uses and potential implications in the fields of chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 736173-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,1,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 736173-15:
(8*7)+(7*3)+(6*6)+(5*1)+(4*7)+(3*3)+(2*1)+(1*5)=162
162 % 10 = 2
So 736173-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H14BrNO.ClH/c18-13-6-3-5-12(10-13)16(19)15-9-8-11-4-1-2-7-14(11)17(15)20;/h1-10,16,20H,19H2;1H
736173-15-2Relevant articles and documents
Synthesis of 2,4-diaryl-3,4-dihydro-2H-naphth[2,1-e][1,3]oxazines and study of the effects of the substituents on their ring-chain tautomerism
Szatmari, Istvan,Martinek, Tamas A.,Lazar, Laszlo,Fueloep, Ferenc
, p. 2231 - 2238 (2004)
A number of 2-(α-amino-Y-substituted-benzyl)-1-naphthol hydrochlorides were prepared by a convenient Mannich-type aminoalkylation. 2,4-Diaryl-3,4-dihydro-2H-naphth-[2,1-e][1,3]oxazines were prepared through the ring-closure reactions of the starting aminonaphthols with aromatic aldehydes, which proved to furnish three-component (ring1-open-ring2) tautomeric mixtures in CDCl3 at 300 K. The electronic effects of the 2-aryl groups on the ratios of the ring-chain tautomeric forms at equilibrium could be described by Equation (1). Study of the effects of substituents X and Y on the tautomeric equilibria [by the aid of the multiple linear regression analysis of Equations (2) and (3)] revealed that the trans-chain equilibrium constants are significantly influenced by the inductive effect (σF) of substituent Y on the 4-phenyl ring. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
