121665-99-4 Usage
Description
4-BROMO-5-ISOPROPYL-2-METHYLBENZENOL, with the molecular formula C10H13BrO, is a white to off-white crystalline powder. It has a melting point of 33-36°C and is recognized for its antimicrobial and antifungal properties. This chemical compound serves as an intermediate in the synthesis of pharmaceuticals and other organic compounds, making it a valuable component in various chemical processes.
Uses
Used in Pharmaceutical Industry:
4-BROMO-5-ISOPROPYL-2-METHYLBENZENOL is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its role in the production of medicinal compounds is crucial, as it contributes to the development of new drugs and therapies.
Used in Personal Care and Household Products Industry:
Leveraging its antimicrobial and antifungal properties, 4-BROMO-5-ISOPROPYL-2-METHYLBENZENOL is used in the production of personal care and household products. It helps maintain hygiene and prevent the growth of harmful microorganisms in these products, ensuring their safety and efficacy.
Safety Precautions:
It is important to handle and use 4-BROMO-5-ISOPROPYL-2-METHYLBENZENOL with caution due to its potential to cause irritation to the skin, eyes, and respiratory system if not properly managed. Adequate safety measures should be taken during its use to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 121665-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,6 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121665-99:
(8*1)+(7*2)+(6*1)+(5*6)+(4*6)+(3*5)+(2*9)+(1*9)=124
124 % 10 = 4
So 121665-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BrO/c1-6(2)8-5-10(12)7(3)4-9(8)11/h4-6,12H,1-3H3
121665-99-4Relevant articles and documents
Copper(II)-catalyzed aromatization followed by bromination of cyclohexenones leading to phenols and bromophenols
Tong, Hung-Chun,Reddy, K. Rajender,Liu, Shiuh-Tzung
, p. 3256 - 3261 (2014/06/09)
Conversion of substituted cyclohexenones into the corresponding phenols can be achieved using copper acetate as the catalyst in the presence of LiBr and CF3COOH under oxygen. With the use of excess LiBr, electrophilic aromatic bromination afforded the corresponding bromophenol under similar catalytic conditions. Copyright
The Chemistry of Terpenes. Part 27.1 The Halogenation of (+)-Thujone and of (-)-Carvotanacetone, and the Stereochemistry and Mechanism of Formation of 'Tribromothujone'
Shannon, Patrick V.R.,Dowsett, Marion
, p. 1527 - 1536 (2007/10/02)
The groos structure and precise stereochemistry of 'tribromothujone' have been identified; its adjacent bromine atoms are cis-orientated.The mechanism of its formation is discussed.A number of halogenated compounds derived from (+)-thujone have been obtained and their absolute configurations determined. (-)-Carvotanacetone dibromide and two tribromides have stereochemically identified.
