174913-08-7 Usage
Uses
Used in Organic Synthesis:
2-bromo-1-chloro-3-methoxybenzene is used as a building block in organic synthesis for the production of various organic compounds. Its unique structure allows for the creation of a wide range of molecules, making it a valuable component in the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-bromo-1-chloro-3-methoxybenzene is used as a key intermediate in the synthesis of drugs. Its presence in the molecular structure can contribute to the desired pharmacological properties of the final product, aiding in the development of novel therapeutic agents.
Used as a Reagent in Chemical Reactions:
2-bromo-1-chloro-3-methoxybenzene also serves as a reagent in various chemical reactions, facilitating the formation of desired products and playing a crucial role in advancing chemical processes.
Used in the Preparation of Agrochemicals:
2-bromo-1-chloro-3-methoxybenzene is also utilized as a starting material for the preparation of agrochemicals, contributing to the development of effective products for agricultural applications.
Safety Precautions:
It is important to handle 2-bromo-1-chloro-3-methoxybenzene with care, as it can be hazardous if not properly managed. Adequate safety measures should be taken during its storage, use, and disposal to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 174913-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,9,1 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174913-08:
(8*1)+(7*7)+(6*4)+(5*9)+(4*1)+(3*3)+(2*0)+(1*8)=147
147 % 10 = 7
So 174913-08-7 is a valid CAS Registry Number.
174913-08-7Relevant articles and documents
107. Substitution electrophile aromatique dans l'anhydride sulfureux liquide. Etude cinetique de la reaction de bromination d'anisoles monosubstitues. Transmission des effets electroniques et caracteristiques de l'etat de transition
Castellonese, Paul,Villa, Pierre
, p. 1068 - 1077 (2007/10/02)
Reactivity-structure correlations for anisole and eleven of its substituted derivatives established from bromination rate constants in liquid SO2, unlike observations in water, show the reaction to be highly sensitive to substituent effects, (ρ+H2O = -7.1; ρ+SO2 = -10.51).This result is ascribed to the solvation of the methoxy group which decreases the conjugation of para-substituted (ρ+O = -9.70) compared to that of ortho-substituted derivatives (ρ+p = -8.86).The highly solvated transition state lies far from reactants on the reaction coordinate and the positive charge developed in this state is nearly unity.
