5452-69-7 Usage
Description
1-(2-bromoethyl)-4-methylcyclohexane is an organic chemical compound characterized by its chemical formula C9H17Br. It is a cycloalkane derivative featuring a bromine atom attached to a carbon within a two-carbon ethyl chain, and a methyl group attached to the cyclohexane ring. 1-(2-bromoethyl)-4-methylcyclohexane is utilized in organic synthesis and chemical research, serving as a starting material for a variety of reactions and acting as a precursor for the synthesis of other organic compounds. Due to its flammability and potential toxicity, it is crucial to handle this chemical with caution to minimize health and environmental risks.
Uses
Used in Organic Synthesis:
1-(2-bromoethyl)-4-methylcyclohexane is used as a starting material for various chemical reactions in the field of organic synthesis. Its unique structure allows for the creation of a wide range of organic compounds, making it a valuable asset in the development of new chemical products.
Used in Chemical Research:
In the realm of chemical research, 1-(2-bromoethyl)-4-methylcyclohexane is employed as a precursor for the synthesis of other organic compounds. Its versatile structure enables researchers to explore new pathways and mechanisms in chemical reactions, contributing to the advancement of scientific knowledge in the field.
Used in Pharmaceutical Industry:
1-(2-bromoethyl)-4-methylcyclohexane may also find applications in the pharmaceutical industry as a building block for the development of new drugs. Its unique chemical properties can be harnessed to create novel therapeutic agents, potentially leading to breakthroughs in the treatment of various medical conditions.
Used in Chemical Manufacturing:
In the chemical manufacturing industry, 1-(2-bromoethyl)-4-methylcyclohexane is utilized as a key component in the production of various chemicals and materials. Its role as a starting material and precursor allows for the creation of a diverse array of products, driving innovation and growth within the industry.
Check Digit Verification of cas no
The CAS Registry Mumber 5452-69-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5452-69:
(6*5)+(5*4)+(4*5)+(3*2)+(2*6)+(1*9)=97
97 % 10 = 7
So 5452-69-7 is a valid CAS Registry Number.
5452-69-7Relevant articles and documents
Synthesis and antiallergy activity of [1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]pyrimidin-9(3H)-one derivatives. II. 6-Alkyl- and 6-cycloalkylalkyl derivatives
Yokohama,Miwa,Aibara,Fujiwara,Matsumoto,Nakayama,Iwamoto,Mori,Moroi,Tsukada,Isoda
, p. 2391 - 2398 (2007/10/02)
A series of 6-alkyl- or 6-(cycloalkylalkyl)-[1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]pyr imidin-9(3H)-ones 1b-o was synthesized from the corresponding 1,3,4-thiadiazol-5-amines 3b-o and the antiallergic activities of the products were evaluated. Among the compounds 6-(2-cyclohexylethyl)-[1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]p yrimidin-9(3H)-one 1h, whose X-ray crystallographic stereostructure is shown, was found to be a promising new antiallergic agent, which has low toxicity and dual activity as a leukotriene D4 receptor antagonist and as an orally active mast cell stabilizer.
