38603-09-7 Usage
General Description
2,6-DIBROMOANISOLE is an organic compound consisting of a benzene ring with two bromine atoms attached at the 2 and 6 positions and a methoxy group at the 4 position. It is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals due to its versatile reactivity and ability to introduce the bromine functionality. It is also used as a flavor and fragrance ingredient in perfumes, soaps, and cosmetics. However, it is important to handle 2,6-DIBROMOANISOLE with caution, as it is considered a skin and eye irritant and may cause respiratory irritation if inhaled. It is also harmful if swallowed and has the potential to cause environmental damage if not disposed of properly.
Check Digit Verification of cas no
The CAS Registry Mumber 38603-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,0 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38603-09:
(7*3)+(6*8)+(5*6)+(4*0)+(3*3)+(2*0)+(1*9)=117
117 % 10 = 7
So 38603-09-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Br2O/c1-10-7-5(8)3-2-4-6(7)9/h2-4H,1H3
38603-09-7Relevant articles and documents
Catalyst Compounds and Use Thereof
-
, (2011/05/05)
This invention relates to Group 4 catalyst compounds containing di-anionic tridentate nitrogen/oxygen based ligands. The catalyst compounds are useful, with or without activators, to polymerize olefins, particularly a-olefins, or other unsaturated monomers. Systems and processes to oligomerize and/or polymerize one or more unsaturated monomers using the catalyst compound, as well as the oligomers and/or polymers produced therefrom are also provided.
POLYBROMINATED AROMATIC COMPOUNDS. III. SYNTHESIS OF BROMINE-SUBSTITUTED ANISOLES
Shishkin, V. N.,Tanaseichuk, B. S.,Lapin, K. K.,Ivkina, A. A.,Butin, K. P.
, p. 2357 - 2366 (2007/10/02)
Reliable methods were developed for the synthesis of di-, tri-, and tetrabromoanisoles, and all the possible individual isomers were synthesized.The structures of the isomers were proved by alternative synthesis and spectral methods (PMR, IR).It was shown that the published data are incorrect in a number of cases; either the final product was assigned the incorrect structure, or the published methods led to mixture of the various isomers.
