449727-85-9 Usage
Uses
Used in Organic Synthesis:
4-ACETOXY-3-BROMOANISOLE is utilized as a key intermediate in organic synthesis for the preparation of various chemical compounds. Its molecular structure and reactivity make it a versatile building block for a wide range of applications.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-ACETOXY-3-BROMOANISOLE is used as a precursor in the synthesis of various drugs. Its unique chemical properties allow it to be incorporated into the molecular structures of pharmaceuticals, potentially enhancing their therapeutic effects.
Used in Agrochemical Development:
4-ACETOXY-3-BROMOANISOLE also finds application in the agrochemical sector, where it serves as a starting material for the development of new agrochemicals. Its reactivity and structural features are harnessed to create compounds with specific pesticidal or herbicidal properties.
Used in the Production of Fine Chemicals:
4-ACETOXY-3-BROMOANISOLE is employed in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including fragrances, flavors, and specialty chemicals. The versatility of 4-ACETOXY-3-BROMOANISOLE in chemical reactions makes it a valuable component in the creation of these high-quality products.
Check Digit Verification of cas no
The CAS Registry Mumber 449727-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,9,7,2 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 449727-85:
(8*4)+(7*4)+(6*9)+(5*7)+(4*2)+(3*7)+(2*8)+(1*5)=199
199 % 10 = 9
So 449727-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO3/c1-6(11)13-9-4-3-7(12-2)5-8(9)10/h3-5H,1-2H3
449727-85-9Relevant academic research and scientific papers
Counterattack mode differential acetylative deprotection of phenylmethyl ethers: Applications to solid phase organic reactions
Chakraborti, Asit K.,Chankeshwara, Sunay V.
experimental part, p. 1367 - 1370 (2009/07/04)
A counterattack protocol for differential acetylative cleavage of phenylmethyl ether has been developed. The phenylmethyl moiety is liberated as benzyl bromide that is isolated and reused providing advantages in terms of waste minimization/utilization and atom economy. The applicability of this methodology has been extended for solid phase organic reactions with the feasibility of reuse of the solid support.
Palladium-catalyzed couplings to nucleophilic heteroarenes: The total synthesis of (-)-frondosin B
Hughes, Chambers C.,Trauner, Dirk
, p. 9675 - 9686 (2007/10/03)
The total synthesis of (-)-frondosin B, the enantiomer of naturally-occuring (+)-frondosin B, is described, wherein a palladium-catalyzed cyclization is used to establish the tetracyclic ring system of the natural product. Graphical Abstract.
