38397-06-7 Usage
Derivative of naphthalene
A modified version of the naphthalene molecule, which is an organic compound with a fused benzene ring structure.
Hydroxyl group at the 1 position
A hydroxyl (-OH) group is attached to the first carbon atom of the naphthalene molecule, giving it unique properties.
Nitro group at the 6 position
A nitro (-NO2) group is attached to the sixth carbon atom of the naphthalene molecule, further modifying its properties.
Synthesis of organic compounds
1-Hydroxy-6-nitronaphthalene is commonly used as a starting material or intermediate in the production of various organic compounds, such as dyes, pigments, and pharmaceuticals.
Semiconducting properties
1-Hydroxy-6-nitronaphthalene has been found to exhibit semiconducting properties, making it a potential candidate for use in organic electronic devices.
Industrial and technological applications
1-Hydroxy-6-nitronaphthalene plays a significant role in the development and production of various industrial and technological products, including dyes, pigments, pharmaceuticals, and organic electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 38397-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,9 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38397-06:
(7*3)+(6*8)+(5*3)+(4*9)+(3*7)+(2*0)+(1*6)=147
147 % 10 = 7
So 38397-06-7 is a valid CAS Registry Number.
38397-06-7Relevant academic research and scientific papers
Generation and Cyclization of Acyl Radicals from Thiol Esters under Nonreducing, Tin-Free Conditions
Crich, David,Hao, Xiaolin
, p. 5982 - 5987 (2007/10/03)
The preparation of 2-(2-((tert-butyloxycarbonyl)amino)phenyl)ethyl mercaptan from 2-(2-aminophenyl)ethanol is described. This thiol is condensed with a series of suitably unsaturated carboxylic acids to give a series of thiol esters. The Boc group is remo
ARYNIC SPECIES; EFFECT OF SUBSTITUENTS ON THE REACTIVITY OF MONOSUBSTITUTED DEHYDROBENZENES
Gavina, F.,Luis, S. V.,Costero, A. M.
, p. 155 - 166 (2007/10/02)
Evidence is presented demonstrating the existence of free dehydrobenzenes in the thermal decomposition of diaryliodonium-2-carboxylates, and that o-benzyne itself and its 4-methyl-, 4-chloro-, 4-bromo- and 4-nitro-derivatives are generated from insoluble polymer-bound precursors and trapped by a second solid phase in Diels-Alder reactions.Lifetimes for these elusive species are determined.
GENERATION OF MONOSUBSTITUTED o-BENZYNES FROM POLYMERIC REAGENTS VIA HETEROLYTIC FRAGMENTATIONS
Gavina, F.,Luis, S.V.,Gil, P.,Costero, A.M.
, p. 779 - 782 (2007/10/02)
Generation of four 4-substituted o-benzynes by heterolytic fragmentation reactions is demonstrated.
