1049730-10-0 Usage
Uses
Used in Pharmaceutical Industry:
3-Cyclopropyl-benzeneboronic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the formation of carbon-carbon bonds through cross-coupling reactions. Its unique cyclopropyl moiety allows for the development of new molecular structures with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Cyclopropyl-benzeneboronic acid serves as a crucial building block for the creation of novel agrochemicals. Its reactivity in cross-coupling reactions is harnessed to synthesize compounds with improved pesticidal properties, contributing to more effective crop protection strategies.
Used in Organic Synthesis:
3-Cyclopropyl-benzeneboronic acid is utilized as a reagent in organic synthesis, where it plays a pivotal role in the formation of carbon-carbon bonds. Its presence in the synthesis process enhances the development of new molecules and materials with diverse applications across various industries.
Used in Material Science:
3-Cyclopropyl-benzeneboronic acid is employed in material science for the development of innovative materials. Its unique chemical properties, stemming from the cyclopropyl group, make it a valuable component in the synthesis of advanced materials with specific properties tailored for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1049730-10-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,7,3 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1049730-10:
(9*1)+(8*0)+(7*4)+(6*9)+(5*7)+(4*3)+(3*0)+(2*1)+(1*0)=140
140 % 10 = 0
So 1049730-10-0 is a valid CAS Registry Number.
1049730-10-0Relevant articles and documents
Synthetic method of 3-cyclopropyl-benzeneboronic acid
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Paragraph 0027; 0030; 0031; 0034; 0035; 0038, (2019/12/25)
The invention discloses a synthetic method of 3-cyclopropyl-benzeneboronic acid, and belongs to the technical field of organic synthesis. The synthetic method comprises the steps: 3-chlorobromobenzeneand cyclopropylboronic acid serve as starting raw mater
Determination of the absolute configuration of two αvβ6 integrin inhibitors for the treatment of idiopathic pulmonary fibrosis and investigations on the asymmetric 1,4-addition of arylboronic acids to crotonate esters bearing a C4-oxygen substituent
Procopiou, Panayiotis A.,Barrett, Tim N.,Copley, Royston C.B.,Tame, Christopher J.
, p. 1384 - 1393 (2017/11/09)
The absolute configuration of two novel αvβ6 integrin inhibitors was established via degradation to the corresponding C3-aryl substituted butyrolactone. The configuration of the resulting lactones was established by asymmetric synthesis using 1,4-addition of arylboronic acids to butenolide, catalysed by bis(norbornadiene)rhodium (I) tetrafluoroborate in the presence of (R)-BINAP, and confirmed by X-ray crystallography. Studies on arylboronic acid conjugate additions to acyclic crotonate esters bearing a γ-oxygen substituent are also reported. Three Rh catalysts were investigated and the one giving the highest enantioselectivity was bis(norbornadiene)rhodium (I) tetrafluoroborate.
