66788-13-4 Usage
Derivative of benzene
This compound is derived from benzene, which is a basic structure consisting of 6 carbon atoms and 6 hydrogen atoms, forming a hexagonal ring.
Two bromine atoms
2,6-dibromo-1,4-dimethylbenzene contains two bromine atoms, which are heavier and more electronegative than hydrogen atoms, and are attached to the carbon atoms in the benzene ring.
Two methyl groups
This compound also has two methyl groups (CH3) attached to adjacent carbon atoms in the benzene ring, which are alkyl groups consisting of one carbon atom and three hydrogen atoms.
Building block in organic synthesis
2,6-dibromo-1,4-dimethylbenzene is commonly used as a starting material for the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials.
Production of dyes and pigments
Due to its unique molecular structure, this compound is used in the production of dyes and pigments for various applications.
Manufacturing of flavors and fragrances
2,6-dibromo-1,4-dimethylbenzene is also used in the creation of flavors and fragrances for consumer products.
Potential application in electronic devices
This compound has been studied for its potential use in organic light-emitting diodes (OLEDs) and other electronic devices, thanks to its unique molecular structure and properties.
Diverse applications
2,6-dibromo-1,4-dimethylbenzene is an important chemical with a wide range of applications across various industries, including pharmaceuticals, agrochemicals, materials, dyes, pigments, flavors, and fragrances.
Check Digit Verification of cas no
The CAS Registry Mumber 66788-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,8 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66788-13:
(7*6)+(6*6)+(5*7)+(4*8)+(3*8)+(2*1)+(1*3)=174
174 % 10 = 4
So 66788-13-4 is a valid CAS Registry Number.
66788-13-4Relevant articles and documents
Synthesis, reactions, and structural and NMR features of [2.2]metacyclophane monoenes and their tricarbonylchromium and cyclopentadienyliron(+) complexes
Mitchell, Reginald H.,Zhang, Limin
, p. 7140 - 7152 (2007/10/03)
8,16-Dimethyl-, 5,8,13,16-tetramethyl-, and 4,6,8,12,14,16- hexamethyl[2.2]metacyclophanene have been synthesized from the corresponding methyl-substituted 3-thia[3.2]metacyclophane precursors via a Wittig rearrangement-Hofmann elimination procedure. Simp
Reactions of Alkyl-lithium Compounds with Aryl Halides
Huddle, Penelope A.,Perold, Guido W.
, p. 2617 - 2625 (2007/10/02)
Reation of methyl-lithium with tribromophenols and with other aryl polyhalides leads directly to bi- and tri-aryl products. para-Substituents (Y) of 2,6-dibromo-4-Y-phenols promote arylation of substrates by their own lithiation products as Y becomes more electron-withdrawing.An aryne epoxide is not an intermediate in these reactions. 2,4,6-Tribromo-Z-benzenes react to form coupling products when Z can co-ordinate to an introduced ortho-lithium atom or when Z can be directly lithiated.Dimeric aggregation of the organolithium intermediates occurs so as to favor coupling to halogenated substrates.Both polar (ionic) and free-radical pathways are involved.
