113851-99-3 Usage
Molecular structure
The compound has a cyclohexadienone ring with two bromine atoms attached to carbons 2 and 6, a dichloromethyl group attached to carbon 4, and a methyl group attached to carbon 4 as well.
Reactivity
The compound is highly reactive and can undergo various chemical reactions, making it versatile in organic synthesis.
Uses
It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
Importance in research
It is also used in research and development in the fields of organic chemistry and material science.
Safety precautions
Due to its chemical structure and properties, it is important to handle this compound with care and use appropriate safety measures when working with it in a laboratory setting.
Check Digit Verification of cas no
The CAS Registry Mumber 113851-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,8,5 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113851-99:
(8*1)+(7*1)+(6*3)+(5*8)+(4*5)+(3*1)+(2*9)+(1*9)=123
123 % 10 = 3
So 113851-99-3 is a valid CAS Registry Number.
113851-99-3Relevant articles and documents
Bromination of 4-dichloromethyl-4-methylcyclohexa-2,5-dien-1-ones
Gavrilova,Rusetskaya,Gavrilov,Trushkov,Krut'ko
, p. 2729 - 2736 (2008/02/12)
Bromination of 4-dichloromethyl-4-methylcyclohexa-2,5-dien-1-one and 4-dichloromethyl-3,4-dimethylcyclohexa-2,5-dien-1-one has been studied. The reaction conditions required for the formation of mono-, di-, and tribrominated products have been optimized.
