68133-80-2 Usage
Description
(Z)-1,1-Dimethoxy-4-decene, a colorless liquid with the molecular formula C12H24O2, is a chemical compound belonging to the class of dialkoxymethane derivatives. It is primarily utilized as an intermediate in the synthesis of various organic compounds, including fragrances, flavors, and pharmaceuticals. Its versatile structure also makes it a valuable building block in the production of surfactants and other specialty chemicals. Moreover, it has been investigated for its potential as a reagent in organic synthesis and as a precursor for the synthesis of biologically active compounds. Although generally stable under normal conditions, it is essential to handle (Z)-1,1-Dimethoxy-4-decene with care due to its potential to cause irritation and toxicity if mishandled.
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 articles and documents
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.
