70454-10-3 Usage
General Description
2,4-DIBROMO-3-ISOPROPYL-6-METHYLBENZENOL, also known as dibromohydroxytoluene, is an organic compound with the molecular formula C10H12Br2O. It is a white to off-white crystalline solid with a faint, aromatic odor. 2,4-DIBROMO-3-ISOPROPYL-6-METHYLBENZENOL is used as a preservative in personal care products, such as shampoos, soaps, and cosmetics, to prevent the growth of bacteria and fungi. It is also utilized as an antimicrobial agent in industrial processes and pharmaceutical products. Additionally, it is known for its wide spectrum of antimicrobial activity and its effectiveness against various microorganisms. However, 2,4-DIBROMO-3-ISOPROPYL-6-METHYLBENZENOL has been associated with potential health risks and environmental concerns, leading to restrictions on its use in certain countries.
Check Digit Verification of cas no
The CAS Registry Mumber 70454-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70454-10:
(7*7)+(6*0)+(5*4)+(4*5)+(3*4)+(2*1)+(1*0)=103
103 % 10 = 3
So 70454-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12Br2O/c1-5(2)8-7(11)4-6(3)10(13)9(8)12/h4-5,13H,1-3H3
70454-10-3Relevant articles and documents
Total synthesis of (+)-19-deoxyicetexone, (-)-Lcetexone, and (+)-5-epi-icetexone
Majetlch, George,Grove, Jeremy L.
supporting information; experimental part, p. 2904 - 2907 (2009/12/06)
The first asymmetric total syntheses of 19-deoxylcetexone, Icetexone, and 5-epl-Icetexone was achieved from eplmerlc tricyclic dlenes.
Bromination of phenols using an algal bromoperoxidase
Shang Meiling,Okuda,Worthen
, p. 307 - 310 (2007/10/02)
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Reactions of Halogenated o-Quinol Acetates with Isopropylmagnesium Bromide and Di-isopropylmagnesium. Mechanism for Formation of Ethers, Reduction Products, and m-Isopropylphenols
Miller, Bernard,Haggerty, John G.
, p. 1617 - 1619 (2007/10/02)
A mechanism is proposed to account for the nature and the variations in yields of products from reactions of Grignard reagents with halogenated o-quinol acetates.
