21450-90-8 Usage
Uses
Used in Organic Synthesis:
2-METHYL-1-NAPHTHYLMAGNESIUM BROMIDE is used as a reagent for Grignard reactions, which are crucial for the formation of carbon-carbon bonds. Its strong nucleophilic nature allows it to participate in various organic reactions, facilitating the creation of new molecular structures and contributing to the synthesis of a broad spectrum of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-METHYL-1-NAPHTHYLMAGNESIUM BROMIDE is utilized as a key intermediate in the synthesis of complex organic molecules that have potential medicinal applications. Its ability to form carbon-carbon bonds is particularly beneficial in the development of novel drug candidates with unique therapeutic properties.
Used in Chemical Research:
2-METHYL-1-NAPHTHYLMAGNESIUM BROMIDE is employed as a research tool in chemical laboratories to explore new reaction pathways and mechanisms. Its reactivity provides insights into the behavior of organometallic compounds in various chemical contexts, furthering the understanding of organic synthesis and contributing to the advancement of chemical science.
Used in Material Science:
In the field of material science, 2-METHYL-1-NAPHTHYLMAGNESIUM BROMIDE is used as a precursor in the synthesis of novel materials with specific properties. Its role in forming carbon-carbon bonds is essential in creating new polymers, composites, and other materials with tailored characteristics for various applications, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 21450-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,5 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21450-90:
(7*2)+(6*1)+(5*4)+(4*5)+(3*0)+(2*9)+(1*0)=78
78 % 10 = 8
So 21450-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9.BrH.Mg/c1-9-6-7-10-4-2-3-5-11(10)8-9;;/h2-7H,1H3;1H;/q;;+1/p-1/rC11H9BrMg/c1-8-6-7-9-4-2-3-5-10(9)11(8)13-12/h2-7H,1H3
21450-90-8Relevant academic research and scientific papers
Practical Synthesis of 1,1'-Binaphtyl-2-carboxylic Acids via Side Chain Oxidation of 2-Methyl-1,1'-binaphtyls
Miyano, Sotaro,Okada, Shin-ichi,Suzuki, Toshiyuki,Handa, Shigeru,Hashimoto, Harukichi
, p. 2044 - 2046 (2007/10/02)
Four 1,1'-binaphtyl-2-carboxylic acids were obtained in 38-53 percent isolated yield via three-stage oxidation of 2-methyl-1,1'-binaphtyls, that is, i) NBS-bromination to benzylic bromides, ii) treatment with sodium salt of 2-nitropropane to aldehydes, and iii) KMnO4-oxidation to carboxylic acids.
