13720-06-4 Usage
Description
2,6-Dibromonaphthalene is a light yellow solid that serves as an essential raw material and intermediate in various industries, including organic synthesis, pharmaceuticals, and agrochemicals. Its chemical structure allows it to undergo specific reactions, such as with hexylmagnesium bromide to form 2,6-dihexyl-naphthalene.
Uses
Used in Organic Synthesis:
2,6-Dibromonaphthalene is used as a key intermediate for the synthesis of various organic compounds. Its bromine atoms facilitate reactions with other molecules, making it a versatile building block in the creation of complex organic structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-dibromonaphthalene is utilized as a starting material for the development of new drugs. Its unique chemical properties allow for the formation of novel drug candidates with potential therapeutic applications.
Used in Agrochemicals:
2,6-Dibromonaphthalene is also employed in the agrochemical sector as a precursor for the synthesis of various agrochemical products. Its reactivity and stability contribute to the development of effective and environmentally friendly solutions for agricultural needs.
Used in Chemical Research:
As a light yellow solid with distinct chemical properties, 2,6-dibromonaphthalene is a valuable compound for research purposes. It can be used to study various chemical reactions and mechanisms, contributing to the advancement of scientific knowledge in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 13720-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13720-06:
(7*1)+(6*3)+(5*7)+(4*2)+(3*0)+(2*0)+(1*6)=74
74 % 10 = 4
So 13720-06-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H6Br2/c11-9-3-1-7-5-10(12)4-2-8(7)6-9/h1-6H
13720-06-4Relevant articles and documents
Funk,R.L.,Vollhardt,K.P.C.
, p. 833 - 834 (1976)
An improved palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides
Pan, Jun,Wang, Xinyan,Zhang, Yong,Buchwald, Stephen L.
supporting information; experimental part, p. 4974 - 4976 (2011/11/06)
A facile Pd-catalyzed conversion of aryl and vinyl triflates to aryl and vinyl halides (bromides and chlorides) is described. This method allows convenient access to a variety of aryl, heteroaryl, and vinyl halides in good to excellent yields and with greatly simplified conditions relative to our previous report.
Naphthalene derivatives, their production and use
-
, (2008/06/13)
A composition containing a compound of the formula: wherein A is a nitrogen-containing heterocyclic group which may be substituted, R1 is a hydrogen atom, hydrocarbon group which may be substituted, or monocyclic aromatic heterocyclic group which may be substituted, R2 is a hydrogen atom or a lower alkyl group which may be substituted, R3, R4, R5, R6, R7, R8 and R9 are independently a hydrogen atom, a hydrocarbon group which may be substituted, a hydroxy group which may be substituted, a thiol group which may be substituted, an amino group which may be substituted, an acyl group or a halogen atom, a salt thereof or a prodrug thereof has steroid C17,20-lyase inhibitory activity, and is useful for preventing and treating for example, primary cancer of malignant tumor, its metastasis and recurrence thereof.
A Convenient Synthesis of Some (1-Alkylethenyl)arenes and Bis(1-alkylethenyl)arenes
Blatter, Karsten,Schlueter, Arnulf-Dieter
, p. 356 - 359 (2007/10/02)
The title compounds may be prepared in good yields and high isomeric purities (98 + percent) by reaction of 1-alkylethenylmagnesium bromides with bromo- or dibromoarenes, respectively).An improved synthesis of 2,6-dibromonaphthalene and synthesis of 4,9-dibromopyrene are also described.