74104-19-1 Usage
Explanation
The chemical formula for 2,6-dibromo-4-chlorophenol consists of a benzene ring with two bromine atoms at the 2 and 6 positions, a chlorine atom at the 4 position, and a hydroxyl group (OH) attached to the carbon at the 1 position.
Explanation
2,6-dibromo-4-chlorophenol has a solid form that is white or off-white in color.
Explanation
The compound has a noticeable and characteristic smell.
Explanation
2,6-dibromo-4-chlorophenol is used in various industrial processes to control the growth of bacteria, fungi, and other harmful microorganisms.
Explanation
The compound is specifically used to treat wood, preventing decay and damage caused by fungi and other organisms that consume wood.
Explanation
2,6-dibromo-4-chlorophenol can be used in the manufacturing of certain medications, either as a key component or as a starting material in the chemical reactions.
Explanation
The compound serves as a building block or intermediate in the synthesis of other organic compounds, facilitating various chemical reactions and transformations.
Explanation
2,6-dibromo-4-chlorophenol can be harmful to human health, posing risks when ingested, inhaled, or absorbed through the skin.
Explanation
The compound can have negative effects on the environment, including water and soil contamination, and harm to non-target organisms.
Explanation
Due to its toxicity and potential environmental impact, the use, storage, and disposal of 2,6-dibromo-4-chlorophenol are subject to strict regulations and guidelines to minimize risks to human health and the environment.
Appearance
White to off-white solid
Odor
Distinctive
Use as a biocide
Effective at killing or inhibiting the growth of microorganisms
Wood preservative
Protects against fungi and wood-destroying organisms
Production of pharmaceuticals
Used as an active ingredient or precursor in the synthesis of drugs
Organic synthesis intermediate
Used in the preparation of other chemical compounds
Toxicity
Potential health risks
Environmental impact
Potential contamination and ecological damage
Regulation and safe handling
Heavily regulated use and disposal
Check Digit Verification of cas no
The CAS Registry Mumber 74104-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,0 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74104-19:
(7*7)+(6*4)+(5*1)+(4*0)+(3*4)+(2*1)+(1*9)=101
101 % 10 = 1
So 74104-19-1 is a valid CAS Registry Number.
74104-19-1Relevant academic research and scientific papers
Solvent-free bromination reactions with sodium bromide and oxone promoted by mechanical milling
Wang, Guan-Wu,Gao, Jie
experimental part, p. 1125 - 1131 (2012/06/04)
New solvent-free brominations of 1,3-dicarbonyl compounds, phenols, various alkenes including chalcones, azachalcones, 4-phenylbut-3-en-2-one, methyl cinnamate, styrene and 1,3-cyclohexadiene were efficiently achieved by employing sodium bromide and oxone under mechanical milling conditions. The brominated products were obtained in good to excellent yields.
Novel halogenated phenol esters, antimicrobial compositions containing them and their use
-
, (2008/06/13)
Halogenated phenol esters of the formula STR1 wherein X represents chlorine or fluorine and R represents hydrogen, alkyl of 1 to 22 carbon atoms, alkenyl of 2 to 22 carbon atoms, benzyl which is unsubstituted or substituted by chlorine or bromine atoms, o
