5434-55-9 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-chlorophenyl)butan-1-ol is utilized as an intermediate in the synthesis of various drugs, playing a crucial role in the development of anti-inflammatory and anti-cancer medications. Its chemical structure allows for the creation of a range of therapeutic agents that can address these health concerns.
Used in Fragrance and Flavor Industry:
1-(2-chlorophenyl)butan-1-ol also finds application in the production of fragrances and flavors, where its unique properties contribute to the creation of distinct scents and tastes for various consumer products.
Used in Research and Development:
1-(2-chlorophenyl)butan-1-ol serves as a building block for various chemical reactions in research and development settings. Its versatility makes it a valuable component in the exploration of new chemical pathways and the synthesis of novel compounds with potential applications across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5434-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5434-55:
(6*5)+(5*4)+(4*3)+(3*4)+(2*5)+(1*5)=89
89 % 10 = 9
So 5434-55-9 is a valid CAS Registry Number.
5434-55-9Relevant academic research and scientific papers
Hydroxyalkylation, Acylation, Formylation, and Carboxylation of 2-Nitro- and 2-Chloro-1-(trimethylsilyl)benzene
Effenberger, Franz,Spiegler, Wolfgang
, p. 3900 - 3914 (2007/10/02)
The synthetic application of base-catalyzed carbodesilylation of aryltrimethylsilanes is demonstrated in the reactions of 2-nitro- (1a) and 2-chloro-1-(trimethylsilyl)benzene (1b) with aldehydes, ketones, acyl fluorides and carboxylic anhydrides, respectively, dimethylformamide, and carbon dioxide.The corresponding benzenes 3 and 8, (hydroxyalkyl)benzenes 4, 6, and 9, the benzophenones 12, the benzaldehydes 14, and the benzoic acids 17 are obtained in good yields.The new method is a useful alternative to the normal electrophilic substitution or the application of organometallic compounds, respectively, for the synthesis of polysubstituted benzenes.
