1095544-81-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Bromo-2-fluoro-4,5-dimethoxybenzene is used as a building block for the production of pharmaceuticals due to its unique structure and the presence of reactive bromine and fluorine atoms, which can be utilized in various chemical reactions to create new medicinal compounds.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1-Bromo-2-fluoro-4,5-dimethoxybenzene serves as a key intermediate in the synthesis of various agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used as a Reagent in Organic Synthesis:
1-Bromo-2-fluoro-4,5-dimethoxybenzene is used as a reagent in organic synthesis, particularly for nucleophilic substitution and cross-coupling reactions. Its reactive bromine and fluorine atoms make it a valuable component in creating a wide range of organic compounds.
Used in Material Science:
In the field of material science, 1-Bromo-2-fluoro-4,5-dimethoxybenzene has potential applications, including serving as a starting material for the synthesis of various functionalized aromatic compounds, which can be further utilized in the development of new materials with specific properties.
Overall, 1-Bromo-2-fluoro-4,5-dimethoxybenzene is a multifaceted chemical with diverse applications across different industries, particularly in organic chemistry, where its unique structure and reactivity play a crucial role in the synthesis of new compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1095544-81-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,5,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1095544-81:
(9*1)+(8*0)+(7*9)+(6*5)+(5*5)+(4*4)+(3*4)+(2*8)+(1*1)=172
172 % 10 = 2
So 1095544-81-2 is a valid CAS Registry Number.
1095544-81-2Relevant articles and documents
General Synthetic Approach to Rotenoids via Stereospecific, Group-Selective 1,2-Rearrangement and Dual S N Ar Cyclizations of Aryl Fluorides
Matsuoka, Seiya,Nakamura, Kayo,Ohmori, Ken,Suzuki, Keisuke
, p. 1139 - 1156 (2019/02/26)
A general synthetic approach to rotenoids is described, featuring 1) stereospecific, group-selective 1,2-rearrangements of epoxy alcohols, and 2) S N Ar oxy-cyclizations of aryl fluorides. The common intermediate epoxyketone, en route to (-)-rotenone and (-)-deguelin, was prepared from d -araboascorbic acid in five steps. Also described is the conversion of (-)-deguelin into oxidized congeners, (-)-tephrosin and (+)-12a- epi -tephrosin.
1,2,4-TRIAZOLO[4,3-C]PYRIMIDIN-3-ONE AND PYRAZOLO [4,3-E] -1,2,4-TRIAZOLO [4,3-C] PYRIMIDIN-3-ONE COMPOUNDS FOR USE AS ADENOSINE A2A RECEPTOR ANTAGONISTS
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Page/Page column 55, (2009/10/22)
Compounds of the Formula I wherein R1 and R2 together with the carbon atoms to which they are bonded optionally form a further heteroaromatic ring of the formula (II) as well as pharmaceutically acceptable salts, solvates, esters and
2-Alkynyl-and 2-alkenyl-pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists
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Page 35, (2008/06/13)
Compounds having the structural formula I or a pharmaceutically acceptable salt thereof, wherein R is R1, R2, R3, R4 and R5 are H, alkyl or alkoxyalkyl; R6 is H, alkyl, hydroxyalkyl or —CH2F; R7, R8 and R9 are H, alkyl, alkoxy, alkylthio, alkoxyalkyl, halo or —CF3; and Z is optionally substituted aryl, heteroaryl or heteroaryl-alkyl are disclosed. Also disclosed is the use of compounds of formula I in the treatment of central nervous system diseases, in particular Parkinson's disease, alone or in combination with other agents for treating Parkinson's disease, and pharmaceutical compositions comprising them.
