7115-89-1 Usage
Description
2-(Bromomethyl)benzoic acid is an organic compound that features a benzylic bromide and a carboxylic acid functional group. These functional groups allow it to participate in nucleophilic reactions and esterification reactions, respectively, making it a versatile building block in organic synthesis and a potential candidate for various applications.
Uses
Used in Pharmaceutical Industry:
2-(Bromomethyl)benzoic acid is used as a synthetic intermediate for the development of pharmaceutical compounds. Its benzylic bromide and carboxylic acid functional groups enable the formation of new chemical entities through nucleophilic reactions and esterification, contributing to the creation of novel drug candidates with potential therapeutic benefits.
Used in Chemical Synthesis:
2-(Bromomethyl)benzoic acid is used as a key building block in the synthesis of various organic compounds. Its reactive functional groups facilitate the formation of new chemical bonds and the construction of complex molecular structures, which can be applied in a wide range of chemical and material science applications.
Used in Material Science:
2-(Bromomethyl)benzoic acid is used as a component in the development of new materials with specific properties. Its ability to undergo nucleophilic reactions and esterification reactions allows for the creation of materials with tailored characteristics, such as improved stability, reactivity, or selectivity, which can be utilized in various industries, including electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 7115-89-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7115-89:
(6*7)+(5*1)+(4*1)+(3*5)+(2*8)+(1*9)=91
91 % 10 = 1
So 7115-89-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO2/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4H,5H2,(H,10,11)
7115-89-1Relevant articles and documents
Synthesis of 2,3-dihydro-1H-2-benzazepin-1-ones and 3H-2-benzoxepin-1-ones by isocyanide-based multicomponent reaction/Wittig sequence starting from phosphonium salt precursors
Wang, Long,Ren, Zhi-Lin,Ding, Ming-Wu
, p. 641 - 646 (2014)
A one-pot synthesis of multisubstituted 2,3-dihydro-1H-2-benzazepin-1-ones and 3H-2-benzoxepin-1-ones by an I-MCR/Wittig sequence was developed. The reaction of phosphonium salt 3, arylglyoxals 4, amine 5 (or without), and isocyanide 6 produced the 2,3-di
One-Pot Synthesis of 3-(1,2,3,4-Tetrahydroisoquinolin-1-yl)-isoquinolin-1(2 H)-ones by DEAD-Promoted Oxidative Ugi-Wittig -Reaction Starting from Phosphonium Salt Precursors
Zhao, Long,Yang, Mao-Lin,Sun, Mei,Ding, Ming-Wu
supporting information, p. 66 - 69 (2021/11/16)
A new one-pot synthesis of 3-(1,2,3,4-tetrahydroisoquinolin-1-yl)-isoquinolin-1(2H)-ones by DEAD-promoted oxidative Ugi Wittig reaction was developed. The sequential reactions of (2-carboxybenzyl)triphenylphosphonium salts, isocyanides, and N-aryl-1,2,3,4
Phthalide: A direct building-block towards P,O and P,N hemilabile ligands. Application in the palladium-catalysed Suzuki-Miyaura cross-coupling of aryl chlorides
McNulty, James,Keskar, Kunal
supporting information, p. 2404 - 2407 (2013/06/05)
The direct synthesis of new hemilabile ligands from the economical, readily available lactone phthalide is described. Pd-complexes of one such ligand were found highly effective in general Suzuki-Miyaura cross-coupling reactions, including deactivated and hindered aryl chlorides. The Royal Society of Chemistry 2013.
