68133-80-2 Usage
Uses
Used in Fragrance and Flavor Industry:
(Z)-1,1-Dimethoxy-4-decene is used as a key intermediate for the synthesis of various fragrances and flavors, contributing to the development of new and improved scents and tastes in the industry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (Z)-1,1-Dimethoxy-4-decene serves as an intermediate in the production of different medicinal compounds, aiding in the development of novel drugs and therapies.
Used in Surfactant Production:
(Z)-1,1-Dimethoxy-4-decene is used as a building block in the synthesis of surfactants, which are essential components in a wide range of consumer products, including detergents, shampoos, and soaps.
Used in Specialty Chemicals:
(Z)-1,1-Dimethoxy-4-decene is also utilized in the production of specialty chemicals, which have applications in various industries such as agriculture, coatings, and plastics.
Used in Organic Synthesis:
(Z)-1,1-Dimethoxy-4-decene has been studied for its potential use as a reagent in organic synthesis, offering new possibilities for the creation of complex molecular structures.
Used in Synthesis of Biologically Active Compounds:
As a precursor for the synthesis of biologically active compounds, (Z)-1,1-Dimethoxy-4-decene plays a crucial role in the development of new bioactive molecules with potential applications in medicine and biotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 68133-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,3 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68133-80:
(7*6)+(6*8)+(5*1)+(4*3)+(3*3)+(2*8)+(1*0)=132
132 % 10 = 2
So 68133-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c1-4-5-6-7-8-9-10-11-12(13-2)14-3/h8-9,12H,4-7,10-11H2,1-3H3/b9-8-
68133-80-2Relevant academic research and scientific papers
Ozonolysis of alkenes and study of the reactions of polyfunctional compounds. XXXIII. Synthesis of (Z)-7-oxo-10-hexadecen-1-ol and its noranalog
Odinokov, V. N.,Botsman, L. P.,Nagaeva, N. A.,Tolstikov, G. A.
, p. 68 - 70 (2007/10/02)
A pathway has been developed for the synthesis of (Z)-7-oxo-10-hexadecen-1-ol, which is a cancer inhibitor, and its noranalog, (Z)-7-oxo-10-pentadecen-1-ol, based on the partial ozonolysis of (Z,Z)-1,5-cyclooctadiene leading to 1,1-dimethoxy-8-tosyloxy-4Z-octene.Subsequent simple transformations of the hydrocarbon skeleton give the desired compounds in five steps.
