60710-39-6 Usage
Description
3-Bromo-4-methylphenol, also known as 2,6-dibromotoluene, is an organic compound with the chemical formula C7H7BrO. It is an off-white crystalline substance that serves as a crucial intermediate in various chemical reactions and holds significant importance in the fields of organic synthesis, pharmaceuticals, agrochemicals, and dyestuff.
Uses
Used in Organic Synthesis:
3-Bromo-4-methylphenol is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for a wide range of reactions, making it a versatile building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Bromo-4-methylphenol is utilized as a starting material for the synthesis of various drugs and drug candidates. Its chemical properties enable the development of new therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Agrochemicals:
3-Bromo-4-methylphenol is also employed in the agrochemical industry as a raw material for the synthesis of pesticides, herbicides, and other agricultural chemicals. Its incorporation into these products helps improve their efficacy and performance in protecting crops and enhancing agricultural productivity.
Used in Dyestuff Industry:
In the dyestuff industry, 3-Bromo-4-methylphenol is used as a vital component in the production of various dyes and pigments. Its chemical properties contribute to the development of dyes with enhanced colorfastness, brightness, and stability, catering to the diverse needs of the textile and other related industries.
Used in Marine Biology:
3-Bromo-4-methylphenol is a component of the marine alga Polysiphonia Sphaerocarpa, which has potential applications in the field of marine biology. Its presence in this alga may contribute to the development of new bioactive compounds with potential pharmaceutical or biotechnological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 60710-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60710-39:
(7*6)+(6*0)+(5*7)+(4*1)+(3*0)+(2*3)+(1*9)=96
96 % 10 = 6
So 60710-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrO/c1-5-2-3-6(9)4-7(5)8/h2-4,9H,1H3
60710-39-6Relevant articles and documents
Synthesis of Polysubstituted Meta-Halophenols by Anion-Accelerated 2π-Electrocyclic Ring Opening
Staudt, Markus,S?lling, Theis,Bunch, Lennart
supporting information, p. 10941 - 10947 (2021/06/16)
Disrotatory – thermally allowed – 2π-electrocyclic ring-opening reactions require high temperatures to proceed. Herein, we report the first anion-accelerated 2π-electrocyclic ring opening of 6,6-dihalobicyclo[3.1.0]hexan-2-ones at low temperature to give the corresponding meta-halophenols in good to high yields (18 examples, 29–92 % yield, average: 65 %). Many of the phenols have unconventional substitution patterns and are reported here for the first time. Furthermore, the strength of the methodology was shown by the total synthesis of the densely functionalized phenolic natural product caramboxin (isolated as the lactam dehydrate). The reaction mechanism underlying the anion-acceleration was investigated in an ab initio study, which concluded that base-mediated proton abstraction anti to the concurrently departing endo-bromine was the initiating step in an overall concerted reaction mechanism leading directly to the meta-halophenol.
Magnolol dimer-derived fragments as PPARγ-selective probes
Dreier, Dominik,Resetar, Mirta,Temml, Veronika,Rycek, Lukas,Kratena, Nicolas,Schnürch, Michael,Schuster, Daniela,Dirsch, Verena M.,Mihovilovic, Marko D.
, p. 7019 - 7028 (2018/10/17)
Partial agonists of the transcription factor PPARγ (peroxisome proliferator-activated receptor γ) have shown potential for the treatment of metabolic and inflammatory conditions and novel activators serve as valuable tool and lead compounds. Based on the
Explorations of the solubilizing effectiveness of CH3OCH2CH2O substituents in the photocyclizations of some 1,2-diarylethylenes to [n]phenacenes
Bohen, Alyssa A.,Mullane, Kimberly C.,Bohen, Joseph M.,Mallory, Clelia W.,Mallory, Frank B.
, p. 3342 - 3345 (2015/03/18)
We have previously published many photocyclizations of 1,2-diarylethylenes to produce zig-zag aromatic ring systems with n = 5, 7, and 11 fused benzene rings. We invented the name [n]phenacenes for these compounds. To increase their solubilities we attach
