868366-91-0 Usage
Physical state
Colorless liquid HCAL is a liquid without color, which is an important characteristic for its applications in various industries.
Odor
Strong, sweet The strong, sweet odor of HCAL contributes to its use in the production of fragrances and perfumes.
Common uses
a. Production of fragrances and perfumes HCAL is used to enhance the olfactory properties of perfumes.
b. Intermediate in pharmaceutical synthesis HCAL is used as an intermediate in the synthesis of various pharmaceutical compounds.
c. Fixative in fragrance formulations HCAL is often used as a fixative to improve the longevity of fragrances.
d. Flavoring agent in the food industry HCAL is used as a flavoring agent in food products.
e. Synthesis of fine chemicals and agrochemicals HCAL has applications in the synthesis of various specialty chemicals and agrochemicals.
Safety precautions
Potentially hazardous substance HCAL should be handled with caution and used and stored according to proper safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 868366-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,3,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 868366-91:
(8*8)+(7*6)+(6*8)+(5*3)+(4*6)+(3*6)+(2*9)+(1*1)=230
230 % 10 = 0
So 868366-91-0 is a valid CAS Registry Number.
868366-91-0Relevant academic research and scientific papers
Intramolecular additions of various π-nucleophiles to chemoselectively activated amides and application to the synthesis of (±)-tashiromine
Belanger, Guillaume,Larouche-Gauthier, Robin,Menard, Frederic,Nantel, Miguel,Barabe, Francis
, p. 704 - 712 (2007/10/03)
Vilsmeier-Haack type cyclizations proved to be particularly efficient for generating parts of the polycyclic cores of many alkaloids, although only monocyclizations have so far been reported. With the goal of rapidly and efficiently constructing polycycli
Addition of tethered nonaromatic carbon nucleophiles to chemoselectively activated amides
Belanger, Guillaume,Larouche-Gauthier, Robin,Menard, Frederic,Nantel, Miguel,Barabe, Francis
, p. 4431 - 4434 (2007/10/03)
(Chemical Equation Presented) In an effort to develop new ways of synthesizing polycyclic alkaloids, we successfully added silyl enol ethers, allylsilanes, and enamines to iminium ions generated from amides. Because of their higher oxidation state, such i
