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(1-methoxynaphthalen-2-yl)boronic acid is a versatile chemical compound used in organic synthesis and medicinal chemistry, characterized by a boronic acid group attached to a naphthalene ring with a methoxy group at position 1. (1-methoxynaphthalen-2-yl)boronic acid is known for its wide range of applications and its ability to selectively bond with certain biological targets, making it a valuable component in the development of targeted therapies for various diseases.

252670-79-4

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252670-79-4 Usage

Uses

Used in Organic Synthesis:
(1-methoxynaphthalen-2-yl)boronic acid is used as a reagent in Suzuki cross-coupling reactions for the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (1-methoxynaphthalen-2-yl)boronic acid serves as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs with improved therapeutic properties.
Used in Material Science:
(1-methoxynaphthalen-2-yl)boronic acid is utilized as a building block in the development of novel materials, thanks to its unique chemical structure and reactivity.
Used in Targeted Therapies Development:
The selective bonding capability of the boronic acid group in (1-methoxynaphthalen-2-yl)boronic acid makes (1-methoxynaphthalen-2-yl)boronic acid useful in the development of targeted therapies for various diseases, potentially improving treatment outcomes and reducing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 252670-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,6,7 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 252670-79:
(8*2)+(7*5)+(6*2)+(5*6)+(4*7)+(3*0)+(2*7)+(1*9)=144
144 % 10 = 4
So 252670-79-4 is a valid CAS Registry Number.

252670-79-4Relevant academic research and scientific papers

Chirality sensing of amines, diamines, amino acids, amino alcohols, and α-hydroxy acids with a single probe

Bentley, Keith W.,Nam, Yea G.,Murphy, Jaslynn M.,Wolf, Christian

, p. 18052 - 18055 (2014/01/06)

A stereodynamic probe for determination of the absolute configuration and enantiomeric composition of chiral amines, diamines, amino alcohols, amino acids, and α-hydroxy carboxylic acids is described. The chirality sensing is based on spontaneous asymmetric transformation of the first kind with stereolabile binaphtholate boron and zinc complexes. The substrate binding and chiral amplification processes yield a distinctive chiroptical sensor output at high wavelength that can be used for rapid and accurate ee detection of minute sample amounts.

Novel 3-aminochromans as potential pharmacological tools for the serotonin 5-HT7 receptor

Holmberg, Paer,Tedenborg, Lars,Rosqvist, Susanne,Johansson, Anette M.

, p. 747 - 750 (2007/10/03)

The synthesis of novel C6-aryl substituted derivatives of 3-(dimethylamino)chroman is described. The novel derivatives display 5-HT 7 receptor affinities that varies from nM to μM, indicating that this small set of derivatives constitute a nove

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