855400-66-7 Usage
Description
3-Bromo-5-methoxyphenol, also known as 3-bromo-5-methoxyphenol, is a chemical compound with the molecular formula C7H7BrO2. It is a white to off-white solid that is commonly used as an intermediate in organic synthesis. The presence of bromo and methoxy groups on the phenol ring makes it a versatile starting material for creating diverse molecular architectures, which is valuable in various applications.
Uses
Used in Pharmaceutical Synthesis:
3-Bromo-5-methoxyphenol is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of diverse molecular architectures, which is essential in drug discovery.
Used in Agrochemical Production:
In the agrochemical industry, 3-Bromo-5-methoxyphenol is used as a precursor in the production of various agrochemicals, contributing to the development of effective and safe products for agricultural use.
Used in Chemical Research:
3-Bromo-5-methoxyphenol serves as a reagent in chemical research, aiding scientists in understanding and advancing the field of organic chemistry through its unique properties and reactivity.
Used in Fine Chemicals Synthesis:
As an intermediate, 3-Bromo-5-methoxyphenol is used in the synthesis of other fine chemicals, which are important in various industries, including fragrances, dyes, and specialty chemicals.
Used in Antimicrobial Compounds Development:
3-Bromo-5-methoxyphenol is used as a starting material for developing novel antimicrobial compounds due to its inherent antimicrobial properties, which can be harnessed to create new treatments and preventive measures against microbial infections.
Used in Antioxidant Compounds Development:
With its antioxidant properties, 3-Bromo-5-methoxyphenol is utilized in the development of new antioxidant compounds, which have potential applications in various industries, including pharmaceuticals, cosmetics, and food preservation.
Used in Materials Science:
3-Bromo-5-methoxyphenol's potential applications in materials science are being explored, where its unique structure and properties could contribute to the development of new materials with specific characteristics and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 855400-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,4,0 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 855400-66:
(8*8)+(7*5)+(6*5)+(5*4)+(4*0)+(3*0)+(2*6)+(1*6)=167
167 % 10 = 7
So 855400-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrO2/c1-10-7-3-5(8)2-6(9)4-7/h2-4,9H,1H3
855400-66-7Relevant articles and documents
Total synthesis of decarboxyaltenusin
Warmuth, Lucas,Wei?, Aaron,Reinhardt, Marco,Meschkov, Anna,Schepers, Ute,Podlech, Joachim
supporting information, p. 224 - 228 (2021/02/26)
The total synthesis of decarboxyaltenusin (5'-methoxy-6-methyl-[1,1'-biphenyl]-3,3',4-triol), a toxin produced by various mold fungi, has been achieved in seven steps in a yield of 31% starting from 4-methylcatechol and 1-bromo-3,5-dimethoxybenzene, where
Total Synthesis of Citreochlorol Monochloro Analogues via a Catalytically Enantioselective Carbonyl Allylation
Hsieh, Bing-Han,Lin, Cheng-Kun,Wu, Chun-Fu
, (2021/11/22)
An efficient synthetic route to citreochlorol analogues, halogenated polyketide secondary metabolites, is described. The key features are Krische s enantioselective carbonyl allylation, IBr-promoted cyclization, and regioselective epoxide opening. The importance of the route lies in accessing a versatile epoxy ether that enables the formation of citreochlorol monochloro derivatives.
Synthesis of Benzyl Amines via Copper-Catalyzed Enantioselective Aza-Friedel-Crafts Addition of Phenols to N -Sulfonyl Aldimines
Shikora, Jonathan M.,Chemler, Sherry R.
supporting information, p. 2133 - 2137 (2018/04/30)
A new copper-catalyzed enantioselective aza-Freidel-Crafts reaction between phenols and N-sulfonyl aldimines that provides chiral secondary benzylamines in good to excellent yields and excellent enantioselectivities (up to 99% ee) is disclosed. In particular, excellent scope with alkylimines was observed for the first time. The synthetic utility of the products was demonstrated in the first enantioselective synthesis of a dual orexin receptor antagonist, a compound that contains an amine-bearing stereocenter adjacent to a bis-ortho-functionalized arene.
