7012-38-6 Usage
Uses
Used in Organic Synthesis:
Cyclohexane, 1-chloro-2-(2-chloroethoxy)is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of products, making it a valuable component in the development of new chemical entities.
Used in Chemical Research:
Cyclohexane, 1-chloro-2-(2-chloroethoxy)serves as a research tool in the study of chemical reactions and mechanisms, particularly in the context of cycloalkane chemistry and chlorination reactions. It helps researchers understand the reactivity and behavior of similar compounds, contributing to the advancement of chemical knowledge.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Cyclohexane, 1-chloro-2-(2-chloroethoxy)is used as a building block for the development of new drugs. Its structural features can be incorporated into drug molecules to impart specific biological activities or improve pharmacokinetic properties.
Used in Chemical Industry:
Cyclohexane, 1-chloro-2-(2-chloroethoxy)is employed as a solvent in certain chemical processes, where its ability to dissolve a variety of substances is beneficial. Additionally, it may be used as an intermediate in the production of other chemical products, such as plastics and polymers.
Used in Solvent Applications:
Cyclohexane, 1-chloro-2-(2-chloroethoxy)is used as a solvent in various industrial processes due to its ability to dissolve a range of materials. Its solubility properties make it a useful component in the formulation of products that require specific solubility characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 7012-38-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7012-38:
(6*7)+(5*0)+(4*1)+(3*2)+(2*3)+(1*8)=66
66 % 10 = 6
So 7012-38-6 is a valid CAS Registry Number.
7012-38-6Relevant academic research and scientific papers
Dulcere,Rodriguez
, p. 399 - 405 (1993)
An investigation of the cohalogenation-dehydrohalogenation sequence as a method for the preparation of allyl vinyl ethers from simple olefins has been performed. Alkenes 1a-k react with bromide or chloride in the presence of ethylene oxide at -80°C to for
REACTION OF PLEFINS WITH SULFURYL CHLORIDE AND CYCLIC RTHERS: AN EFFICIENT SYNTHESIS OF α-CHLOROALKYL ω-CHLOROALKYL ETHERS
Joseph, Sajan P.,Keshavamurthy, K. S.,Dhar, D. N.
, p. 889 - 896 (2007/10/02)
Olefins react with sulfuryl chloride in presence of cyclic ethers to form the corresponding α-chloroalkyl ω-chloroalkyl ethers.
