108052-76-2 Usage
Description
4-(Bromomethyl)-benzoic acid, 1,1-dimethylethyl ester is a chemical compound belonging to the ester class, characterized by the presence of a bromomethyl group (-CH2Br) attached to the fourth carbon of the benzene ring in the benzoic acid molecule, along with a 1,1-dimethylethyl ester group. It is widely utilized in the field of organic chemistry as a reagent or intermediate in the synthesis of other organic compounds. Due to its potential health and safety risks, it should be handled with caution.
Uses
Used in Organic Chemistry:
4-(Bromomethyl)-benzoic acid, 1,1-dimethylethyl ester is used as a reagent for various chemical reactions, facilitating the synthesis of a range of organic compounds. Its unique structure, featuring a bromomethyl and a 1,1-dimethylethyl ester group, makes it a valuable component in the creation of new molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(Bromomethyl)-benzoic acid, 1,1-dimethylethyl ester is used as an intermediate in the development of new drugs. Its ability to participate in various chemical reactions allows for the creation of diverse drug candidates with potential therapeutic benefits.
Used in Chemical Research:
4-(Bromomethyl)-benzoic acid, 1,1-dimethylethyl ester is also employed in chemical research as a model compound to study the properties and reactivity of esters and bromomethyl groups. This helps researchers gain insights into the behavior of similar compounds and develop new synthetic strategies and applications.
Used in Material Science:
In the field of material science, 4-(Bromomethyl)-benzoic acid, 1,1-dimethylethyl ester is utilized in the synthesis of novel materials with specific properties, such as polymers, coatings, and adhesives. Its versatility in chemical reactions enables the development of materials with tailored characteristics for various applications.
Overall, 4-(Bromomethyl)-benzoic acid, 1,1-dimethylethyl ester is a versatile chemical compound with a wide range of applications in different industries, including organic chemistry, pharmaceuticals, chemical research, and material science. Its unique structure and reactivity make it an essential component in the synthesis of various organic compounds and the development of new materials and drugs. However, due to its potential health and safety risks, it is crucial to handle this compound with care and follow appropriate safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 108052-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,5 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108052-76:
(8*1)+(7*0)+(6*8)+(5*0)+(4*5)+(3*2)+(2*7)+(1*6)=102
102 % 10 = 2
So 108052-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H15BrO2/c1-12(2,3)15-11(14)10-6-4-9(8-13)5-7-10/h4-7H,8H2,1-3H3
108052-76-2Relevant articles and documents
Investigation of the Stereoselective Synthesis of the Indane Dimer PH46A, a New Potential Anti-inflammatory Agent
Cumming, Graham R.,Zhang, Tao,Scalabrino, Gaia,Frankish, Neil,Sheridan, Helen
, p. 1972 - 1979 (2017)
PH46A, belonging to a class of 1,2-Indane dimers, has been developed by our research group as a potential therapeutic agent for the treatment of inflammatory and autoimmune diseases. The initial synthetic route to PH46A gave a low overall yield, due in la
Novel nicotinoid structures for covalent modification of wood: An environmentally friendly way for its protection against insects
Acker, Sophie,Kaufmann, Dieter E.,Namyslo, Jan C.,Plarre, Rudy,S?ftje, Martin
, p. 15726 - 15733 (2020/05/13)
Timber is constantly exposed to environmental influences under outdoor conditions which limits its lifetime and usability. In order to counteract the damaging processes caused by insects, we have developed a novel and more environmentally friendly method to protect wood materials via covalent modification by organic insecticides. Starting with an important class of synthetic insecticides which are derived from the natural insecticide nicotine, various new carboxylic acid derivatives of imidacloprid were made accessible. These activated neonicotinoids were utilized for the chemical modification of wood hydroxy groups. In contrast to conventional wood preservation methods in which biocides are only physically bound to the surface for a limited time, the covalent fixation of the preservative guarantees a permanent effect against wood pests, demonstrated in standardized biological tests. Additionally, the environmental interaction caused by non-bound neonicotinoids is significantly reduced, since both, a smaller application rate is required and leaching of the active ingredient is prevented. By minimizing the pest infestation, the lifetime of the material increases while preserving the natural appearance of the material.
3-(1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF
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Paragraph 0857; 0859, (2019/03/08)
The present disclosure provides a compound of Formula (I′): or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein R1, R2, Rx, X1, n, n1, and q are as defined herein, and methods of making and using same.
Picolinamide oligomers, preparation method and applications thereof
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Paragraph 0047; 0052, (2018/08/28)
The invention belongs to the technical field of membrane separation, and more specifically relates to picolinamide oligomers, a preparation method and applications thereof. The picolinamide oligomerscomprise the following characteristics: 1. the oligomers
