100477-85-8 Usage
Molecular weight
263.93 g/mol
Appearance
White or pale yellow crystalline solid
Functional groups
Halogenated phenol, methyl group
Bromine positions
2 and 6 on the benzene ring
Methyl position
3 on the benzene ring
Applications
Synthesis of pharmaceuticals, agrochemicals, and intermediates
Applications
The resulting compound has applications in the production of pesticides, fungicides, and pharmaceutical intermediates.
Formation of a stable compound
The mixture of 2,6-dibromo-3-methyl-phenol and methylamine forms a stable and useful compound.
Importance
The mixture is an essential component in the manufacturing of various agricultural and pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 100477-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,7 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100477-85:
(8*1)+(7*0)+(6*0)+(5*4)+(4*7)+(3*7)+(2*8)+(1*5)=98
98 % 10 = 8
So 100477-85-8 is a valid CAS Registry Number.
100477-85-8Relevant articles and documents
Ortho-Specific Bromination of Phenols
Schmitz, Ernst,Pagenkopf, Ingeborg
, p. 998 - 1006 (2007/10/02)
Phenol as well as 3-substituted phenols are brominated exclusively in the ortho positions by N.N-dibromomethylamine, yielding 2.6-dibrominated phenols in excellent yields.Phenols bearing an ortho-substituent need N-bromomethylamine as the brominating agent to take up one bromine atom into the free ortho-position. para-Bromination is not observed in either case. 1-Naphthol gives 2-bromo-1-naphthol, 8-hydroxyquinoline gives 7-bromo-8-hydroxyquinoline with 80percent and 98percent yield respectively. ortho-Specific chlorination of phenols was carried out in some cases using N-chloro-alkylamines.
