17612-50-9 Usage
Uses
Used in Chemical Industry:
(1Z,5Z)-cycloocta-1,5-diene is used as a diene in organic synthesis for the production of various polymers and resins. Its reactivity allows it to form a wide range of chemical compounds, making it a valuable component in the chemical industry.
Used in Specialty Chemicals Manufacturing:
(1Z,5Z)-cycloocta-1,5-diene is used as a precursor in the manufacturing of various specialty chemicals. Its unique properties and reactivity enable the production of specific chemical compounds that are used in different industries.
Used in Research and Development:
(1Z,5Z)-cycloocta-1,5-diene is used as a research compound in the development of new chemical processes and products. Its reactivity and ability to form various chemical compounds make it an important tool for researchers in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 17612-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,1 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17612-50:
(7*1)+(6*7)+(5*6)+(4*1)+(3*2)+(2*5)+(1*0)=99
99 % 10 = 9
So 17612-50-9 is a valid CAS Registry Number.
InChI:InChI=1S/C8H12/c1-2-4-6-8-7-5-3-1/h1-2,7-8H,3-6H2/b2-1+,8-7+
17612-50-9Relevant academic research and scientific papers
Discontinuous pressure effect upon enantiodifferentiating photosensitized isomerization of cyclooctene
Kaneda, Masayuki,Asaoka, Sadayuki,Ikeda, Haruhiko,Mori, Tadashi,Wada, Takehiko,Inoue, Yoshihisa
, p. 1272 - 1273 (2007/10/03)
A hydrostatic pressure of up to 750 MPa induced discontinuous changes in the enantiomeric excess of the (E)-isomer obtained in the enantiodifferentiating photoisomerization of (Z)-cyclooctene and (Z,Z)-cycloocta-1,5-diene, sensitized by chiral benzene-1,2,4,5-tetracarboxylates; indicating a switching of the enantiodifferentiation mechanism, which is attributable to dramatic conformational changes of chiral alkoxycarbonyl auxiliaries at a specific pressure.
