6803-40-3 Usage
Description
Thiocyanic acid hexyl ester, also known as hexyl thiocyanate, is an organic compound characterized by the chemical formula C7H13NS. It presents as a colorless to pale yellow liquid with a distinct pungent odor and is insoluble in water. Thiocyanic acid hexyl ester is recognized for its versatile applications across different industries.
Uses
Used in Flavor and Fragrance Industry:
Thiocyanic acid hexyl ester serves as a flavor and fragrance ingredient, particularly in the food and cosmetic sectors. It is valued for its ability to impart a fruity, pineapple-like scent, enhancing the sensory experience of products.
Used in Chemical Synthesis:
In the realm of chemical synthesis, thiocyanic acid hexyl ester operates as a reagent. Its chemical properties make it a useful component in the production of various compounds and materials.
Used in Agriculture as a Pesticide:
Thiocyanic acid hexyl ester also finds application in agriculture, where it is utilized as a pesticide. Its properties contribute to controlling and managing pests that can harm crops and reduce agricultural yields.
Safety Considerations:
While thiocyanic acid hexyl ester is considered to have low toxicity, it can be irritating to the eyes, skin, and respiratory system. Therefore, it is essential to handle this compound with caution to minimize potential adverse effects.
Regulatory Status:
Thiocyanic acid hexyl ester is not classified as a carcinogen or a reproductive toxicant, according to current regulatory standards. However, it is always prudent to stay updated with the latest research and guidelines regarding its use and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 6803-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,0 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6803-40:
(6*6)+(5*8)+(4*0)+(3*3)+(2*4)+(1*0)=93
93 % 10 = 3
So 6803-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NS/c1-2-3-4-5-6-9-7-8/h2-6H2,1H3
6803-40-3Relevant articles and documents
Synthesis of hexylselenol and hexylselenides from hexylthiol involving hexylthiolanium salts
Krief, Alain,Dumont, Willy,Robert, Michael
, p. 2601 - 2604 (2008/09/16)
Selenium nucleophiles react regioselectively at the endocyclic or exocyclic carbon of hexylthiolanium salts depending upon the nature of the salt. Georg Thieme Verlag Stuttgart.
