164526-13-0 Usage
Derivative of benzo[1,4]dioxin
Heterocyclic compound
The compound is derived from benzo[1,4]dioxin, which is a heterocyclic compound containing a benzene ring fused to a 1,4-dioxin ring.
Structural features
Amino group and ketone group
The presence of an amino group (-NH2) and a ketone group (C=O) in the structure of the compound contributes to its potential as a building block for the synthesis of various pharmaceuticals and organic compounds.
Potential applications
Pharmaceutical synthesis and organic compounds
Due to its unique structural features, the compound may be used as a building block for the synthesis of various pharmaceuticals and organic compounds.
Medicinal chemistry
Possible applications
The compound may have applications in medicinal chemistry due to its unique structural features and potential biological activities.
Further research
Required to explore potential uses and properties
Additional research and studies are needed to fully understand the potential uses and properties of 1-(7-AMINO-2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-ETHANONE in various fields, such as pharmaceutical development and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 164526-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,5,2 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 164526-13:
(8*1)+(7*6)+(6*4)+(5*5)+(4*2)+(3*6)+(2*1)+(1*3)=130
130 % 10 = 0
So 164526-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-6(12)7-4-9-10(5-8(7)11)14-3-2-13-9/h4-5H,2-3,11H2,1H3
164526-13-0Relevant articles and documents
A new effective route for the synthesis of substituted 2H-indazoles
Mochalov,Khasanov,Trofimova,Fedotov,Zefirov
experimental part, p. 1208 - 1217 (2010/06/12)
A two-stage synthesis of 2H-indazoles has been established, based on consecutive reactions of reduction of 2-alkyl-, 2-cyclopropyl-, and 2-arylcarbonylazobenzenes to phenylazo-substituted benzyl alcohols and intramolecular heterocyclization of the reducti
Simple route to 3-(2-indolyl)-1-propanones via a furan recyclization reaction
Butin, Alexander V.,Smirnov, Sergey K.,Stroganova, Tatyana A.,Bender, Wolfgang,Krapivin, Gennady D.
, p. 474 - 491 (2007/10/03)
A simple route to 1-R-3-(2-indolyl)-1-propanones has been elaborated based on recyclization of 2-(2-aminobenzyl)furan derivatives. Being a modification of the Reissert indole synthesis, our approach employs the furan ring as a source of carbonyl function. This approach is general and allows varying of substituents in aromatic ring as well as in 3-position of indole nucleus.
SYNTHESIS OF 1,3-DIHYDRO-5(R)-7,8-ETHYLENEDIOXY-2H-1,4-BENZO-DIAZEPIN-2-ONES
Mochalov, S. S.,Kosynkin, D. V.,Yudin, I. D.,Atanov, V. N.,Shabarov, Yu. S.,Zefirov, N. S.
, p. 527 - 532 (2007/10/02)
1-Diazepin-2-ones have been prepared from 1,4-benzodioxane for the first time.
