63281-97-0 Usage
Uses
Used in Organic Synthesis:
(E)-1-chlorohex-3-ene is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of a wide range of products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (E)-1-chlorohex-3-ene is utilized as a building block for the development of new drugs. Its reactivity and functional groups enable the formation of complex molecular structures with potential therapeutic applications.
Used in Pesticide and Agrochemical Manufacturing:
(E)-1-chlorohex-3-ene is employed as a starting material or intermediate in the production of pesticides and agrochemicals. Its properties make it suitable for the creation of compounds that can effectively control pests and protect crops.
Environmental Hazard:
(E)-1-chlorohex-3-ene is recognized as a potential environmental hazard due to its toxic and flammable nature. As a result, it is crucial to handle (E)-1-chlorohex-3-ene with care and implement proper safety measures during its production, use, and disposal to minimize its impact on the environment and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 63281-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,8 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63281-97:
(7*6)+(6*3)+(5*2)+(4*8)+(3*1)+(2*9)+(1*7)=130
130 % 10 = 0
So 63281-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H11Cl/c1-2-3-4-5-6-7/h3-4H,2,5-6H2,1H3/b4-3+
63281-97-0Relevant academic research and scientific papers
Enzyme-triggered enantioconvergent transformation of haloalkyl epoxides
Mayer, Sandra F.,Steinreiber, Andreas,Orru, Romano V. A.,Faber, Kurt
, p. 4537 - 4542 (2007/10/03)
Biocatalytic hydrolysis of 2,3-disubstituted rac-cis- and rac-trans-haloalkyl epoxides 1a-8a using the epoxide hydrolase activity of whole bacterial cells furnished the corresponding vicinal diols 1b-8b as intermediates; these (spontaneously) underwent ring closure to yield cyclic products 1c-6c through an enzyme-triggered cascade reaction. In particular, cis-configured substrates (1a, 3a, 5a, 7a) were transformed in an enantioconvergent fashion, which resulted in the formation of single stereoisomeric products in 100% des and up to 92% ees from the racemates.
