737000-93-0 Usage
Uses
Used in Health and Nutrition Industry:
(R)-(-)-2-Heptyl isothiocyanate is used as a bioactive compound for its potential health benefits. It is known for its anticancer properties, which can help in the prevention and treatment of various types of cancer. Additionally, its antimicrobial properties make it a valuable component in the development of natural antimicrobial agents to combat bacterial and fungal infections.
Used in Research and Development:
In the field of research and development, (R)-(-)-2-Heptyl isothiocyanate is used as a chemical compound to study its effects on different organisms. This helps in understanding its potential applications in various scientific and medical contexts, contributing to the advancement of knowledge in these areas.
Used in Agriculture:
(R)-(-)-2-Heptyl isothiocyanate is used as a natural pesticide in the agriculture industry due to its antimicrobial properties. It can help protect crops from harmful bacteria and fungi, promoting healthier plant growth and increased crop yields.
Used in Flavor and Fragrance Industry:
Due to its strong smell, (R)-(-)-2-Heptyl isothiocyanate can be used as a component in the flavor and fragrance industry. It can be utilized in the creation of unique scents for perfumes, candles, and other aromatic products, as well as in the development of flavorings for the food and beverage industry.
Check Digit Verification of cas no
The CAS Registry Mumber 737000-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,7,0,0 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 737000-93:
(8*7)+(7*3)+(6*7)+(5*0)+(4*0)+(3*0)+(2*9)+(1*3)=140
140 % 10 = 0
So 737000-93-0 is a valid CAS Registry Number.
737000-93-0Relevant academic research and scientific papers
Michalski, Oskar,Ciez, Dariusz
, p. 225 - 235 (2013)
Chiral alkyl 2-isothiocyanates have been obtained from enantiopure, aliphatic amines. ECD measurements allowed us to correlate an absolute configuration at C-2 with a sign of the Cotton effect (CE) observed for n-π- transition at the longer-wavelength range of the spectrum. Chirooptical data calculated for all enantiomers were consistent with the measured CE values and indicated that the weak absorption band at 240 nm could give an important information concerning the stereochemistry of simple, chiral isothiocyanates. Optically active esters of 2-isothiocyanatocarboxylic acids, prepared from α-amino acids, showed two absorption bands located over 195 nm. The more intensive band near 200 nm and the weak absorption located at 250 nm were related to n-π- transitions in NCS group. TD DFT calculations carried out for methyl esters of 2-isothiocyanatocarboxylic acids showed the correlation between signs of CE determined for both absorption bands, and the absolute configuration on C-2.
