52897-67-3 Usage
Molecular structure
A benzene ring with two hydroxyl (OH) groups at the 1 and 2 positions, three bromine (Br) atoms at the 3, 4, and 6 positions, and a hydroxymethyl (CH2OH) group at the 5 position.
Physical state
White crystalline solid
Odor
Faint, somewhat phenolic
Primary uses
a. Flame retardant in industrial and consumer products (plastics, textiles, electronic devices)
b. Fungicide
c. Disinfectant
d. Production of pharmaceuticals and dyes
Environmental and health concerns
Potential toxicity and environmental impact
Regulatory status
Use has been regulated in some jurisdictions due to its potential risks
Check Digit Verification of cas no
The CAS Registry Mumber 52897-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,9 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52897-67:
(7*5)+(6*2)+(5*8)+(4*9)+(3*7)+(2*6)+(1*7)=163
163 % 10 = 3
So 52897-67-3 is a valid CAS Registry Number.
52897-67-3Relevant academic research and scientific papers
Total synthesis of the biologically active, naturally occurring 3,4-dibromo-5-[2-bromo-3,4-dihydroxy-6-(methoxymethyl)benzyl]benzene-1,2-diol and regioselective O-demethylation of aryl methyl ethers
Akbaba, Yusuf,Balaydin, Halis Tuerker,Goeksu, Sueleyman,Sahin, Ertan,Menzek, Abdullah
experimental part, p. 1127 - 1135 (2010/08/21)
3,4-Dibromo-5-[2-bromo-3,4-dihydroxy-6-(methoxymethyl)benzyl]benzene-1, 2-diol (2), a natural product, has been synthesized for the first time starting from (3-bromo-4,5-dimethoxyphenyl)methanol (5) in five steps and with an overall yield of 34%. The reaction of some methoxymethyl-substituted aryl methyl ethers with BBr3, followed by the addition of MeOH, afforded the corresponding methoxymethyl-substituted arylphenols in high yields.
