406482-22-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Bromo-4-methoxy-2,3-difluorobenzene is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits. 1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE's reactivity and functional groups enable the formation of diverse molecular structures, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 1-bromo-4-methoxy-2,3-difluorobenzene serves as an essential building block for the production of agrochemicals, such as pesticides and herbicides. Its halogenated nature allows for the creation of compounds with enhanced pesticidal properties, improving crop protection and yield.
Used in Liquid Crystal Industry:
1-Bromo-4-methoxy-2,3-difluorobenzene is utilized in the production of liquid crystals, which are crucial components in display technologies. Its molecular structure contributes to the formation of liquid crystal materials with specific properties, such as temperature stability and electro-optic effects, enhancing the performance of liquid crystal displays.
Used in Dye Industry:
1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE is also employed in the synthesis of dyes, particularly those with halogenated structures. The presence of bromine and fluorine atoms in 1-bromo-4-methoxy-2,3-difluorobenzene imparts unique color characteristics and stability to the resulting dyes, making them suitable for various applications, including textiles, inks, and pigments.
Safety Precautions:
Due to its halogenated nature, 1-bromo-4-methoxy-2,3-difluorobenzene should be handled with caution and proper safety measures. Exposure to 1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE may pose potential health hazards, and therefore, it is essential to follow recommended guidelines for safe handling, storage, and disposal to prevent any adverse effects on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 406482-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,4,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 406482-22:
(8*4)+(7*0)+(6*6)+(5*4)+(4*8)+(3*2)+(2*2)+(1*2)=132
132 % 10 = 2
So 406482-22-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrF2O/c1-11-5-3-2-4(8)6(9)7(5)10/h2-3H,1H3
406482-22-2Relevant articles and documents
FUSED PENTACYCLIC ANTI - PROLIFERATION COMPOUNDS
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Page/Page column 78, (2013/02/28)
The present invention relates to novel compounds of formula (I) wherein X, Q, R1, R2, R3, R4, R5, R6, R7, R8, R21, R22 and R23 are as defined herein. The compounds of formula (I) are inhibitors of telomerase enzyme function and are accordingly useful for the treatment cellular proliferation disorders, such as cancer
Perhydroazulenes - A new class of liquid crystalline materials
Hopf, Henning,Hussain, Zakir,Menon, Rajeev S.,Raev, Vitaly,Jones, Peter G.,Pohl, Ludwig M.
scheme or table, p. 1273 - 1276 (2011/07/06)
A new class of mesogenic compounds, the perhydroazulenes, carrying substituents in their para positions (HAZ derivatives), has been synthesized. The new liquid crystalline materials display a broad enantiotropic nemantic mesophase slightly above room temp
NOVEL ESTROGEN RECEPTOR LIGANDS
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Page/Page column 65, (2009/03/07)
The invention provides a compound of formula (I) or a pharmaceutically acceptable ester, amide, solvate or salt thereof, including a salt of such an ester or amide, and a solvate of such an ester, amide or salt, wherein W, X, Y, Z, R1, R2, R7, R8, R9, R10, R11, R12, R13, R14, R15 and R16 are as defined in the specification. The invention also provides also provides the use of such compounds in the treatment or prophylaxis of a condition associated with a disease or disorder associated with estrogen receptor activity.
