138505-27-8 Usage
Description
4-bromo-1-isopropoxy-2-methoxybenzene is a chemical compound with the molecular formula C10H13BrO2. It is a derivative of 2-methoxyphenol, also known as guaiacol, and contains a bromine atom, an isopropoxy group, and a methoxy group attached to the benzene ring. 4-bromo-1-isopropoxy-2-methoxybenzene is known for its strong aromatic odor and is commonly used in various applications due to its unique chemical properties.
Uses
Used in Organic Synthesis:
4-bromo-1-isopropoxy-2-methoxybenzene is used as a building block in organic synthesis for the creation of various pharmaceuticals and agrochemicals. Its unique structure allows for the formation of complex organic molecules that can be utilized in the development of new drugs and agricultural products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-bromo-1-isopropoxy-2-methoxybenzene serves as a key intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can influence the biological activity and pharmacological properties of the final product, making it a valuable component in drug discovery and development.
Used in Perfume and Fragrance Manufacturing:
4-bromo-1-isopropoxy-2-methoxybenzene is used as a raw material in the manufacturing of perfumes and fragrances due to its strong aromatic odor. Its unique scent profile can be incorporated into various fragrance formulations, contributing to the overall olfactory experience of the final product.
Used in Materials Science:
4-bromo-1-isopropoxy-2-methoxybenzene has potential applications in the field of materials science, where it can be used to develop new materials with specific properties. Its chemical structure may contribute to the creation of materials with unique characteristics, such as improved stability, reactivity, or other desirable traits.
Used as a Chemical Intermediate in Various Industries:
In addition to its direct applications, 4-bromo-1-isopropoxy-2-methoxybenzene also serves as a chemical intermediate in various industries. Its versatility allows it to be used in the production of a wide range of products, from specialty chemicals to advanced materials, making it a valuable component in the chemical manufacturing process.
Check Digit Verification of cas no
The CAS Registry Mumber 138505-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,0 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138505-27:
(8*1)+(7*3)+(6*8)+(5*5)+(4*0)+(3*5)+(2*2)+(1*7)=128
128 % 10 = 8
So 138505-27-8 is a valid CAS Registry Number.
138505-27-8Relevant articles and documents
Synthesis of lamellarin alkaloids using orthoester-masked α-keto acids
Shirley, Harry J.,Koyioni, Maria,Muncan, Filip,Donohoe, Timothy J.
, p. 4334 - 4338 (2019/04/17)
Pyruvic acid and other α-keto acids are frequently encountered as intermediates in metabolic pathways, yet their application in total synthesis has met with limited success. In this work, we present a bioinspired strategy that utilizes highly functionaliz
Short synthesis and antimalarial activity of fagaronine
Rivaud,Mendoza,Sauvain,Valentin,Jullian
experimental part, p. 4856 - 4861 (2012/08/29)
Herein, we report a new synthesis of fagaronine 1, inspired by the synthesis reported by Luo for nornitidine. The in vitro biological activity of fagaronine against malaria on several chloroquine-sensitive and resistant Plasmodium falciparum strains was c
Synthesis of Larreantin, a Cytotoxic Napththoquinoid Sesquilignan from Larrea tridentata
Comber, Mark F.,Sargent, Melvyn V.
, p. 2783 - 2787 (2007/10/02)
Larreantin 1, a biogenetically unique cytotoxic naphthoquinoid sesquilignan has been synthesized by a convergent route.The key intermediate was 4,5-dihy
