383869-51-0 Usage
Uses
Used in Pharmaceutical Industry:
4-Bromo-1-ethoxy-2-nitrobenzene is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Bromo-1-ethoxy-2-nitrobenzene is utilized as an intermediate in the production of agrochemicals, aiding in the creation of compounds that can protect crops from pests and diseases.
Used in Dye Industry:
4-Bromo-1-ethoxy-2-nitrobenzene is employed as a building block in the synthesis of dyes, contributing to the development of colorants for various applications, including textiles and other industrial uses.
Used in Organic Synthesis:
As a versatile building block, 4-Bromo-1-ethoxy-2-nitrobenzene is used in organic synthesis to construct a wide range of organic compounds for research and commercial purposes.
Used in Chemical Reactions as a Reagent:
4-Bromo-1-ethoxy-2-nitrobenzene serves as a reagent in various chemical reactions, facilitating specific transformations and processes in the synthesis of target molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 383869-51-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,8,6 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 383869-51:
(8*3)+(7*8)+(6*3)+(5*8)+(4*6)+(3*9)+(2*5)+(1*1)=200
200 % 10 = 0
So 383869-51-0 is a valid CAS Registry Number.
383869-51-0Relevant articles and documents
PIPERAZINE DERIVATIVES USEFUL FOR THE TREATMENT OF GASTROINTESTINAL DISORDERS
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Page/Page column 48, (2010/02/15)
The invention provides compounds of formula (I) or pharmaceutically acceptable salts thereof, wherein Ra, Rb, Rc, Rd, Re, Rf and Y are as defined in the specification. The compounds are partial or full agonists at the growth hormone secretagogue (GHS) receptors . Pharmaceutical compositions comprising the compounds, methods of preparing the compounds, uses of the compounds and methods involving the compounds are also provided.
Kinetic studies of the reactions of some phenols and alkyl aryl ethers with dinitrogen pentoxide in perfluorocarbon solvents
Crampton,Gibbons,Millar
, p. 1662 - 1665 (2007/10/03)
The reaction of dinitrogen pentoxide in perfluorocarbon solvents with phenols and alkyl aryl ethers carrying halogeno ring-substituents results in nitrodehydrogenation. Rate measurements show that the preferred orientation of nitration is ortho > para > meta to the hydroxy group; the kinetic isotope effect, kH/kD, has a value close to unity. Phenols show considerably higher reactivity than similarly substituted alkyl phenyl ethers, and a mechanism is suggested involving initial interaction of N2O5 with the hydroxy function followed by reaction via cyclic transition states.
