194154-02-4 Usage
Uses
Used in Chemical Synthesis:
Ethanol, 2-(2-isothiocyanatoethoxy)is used as a reagent or intermediate in chemical synthesis for various applications. Its unique chemical structure allows it to be a versatile building block in the creation of new compounds and materials.
Used in Antimicrobial Applications:
Ethanol, 2-(2-isothiocyanatoethoxy)has been studied for its potential antimicrobial properties. It can be used as a disinfectant or preservative in various industries, such as food and beverage, pharmaceuticals, and cosmetics, to inhibit the growth of harmful microorganisms.
Used in Antioxidant Applications:
Ethanol, 2-(2-isothiocyanatoethoxy)has also been studied for its potential antioxidant properties. It can be used as an additive in various products to prevent oxidation and spoilage, thereby extending their shelf life and maintaining their quality.
Used in Laboratory Research:
Ethanol, 2-(2-isothiocyanatoethoxy)is used in laboratory research for studying its chemical properties and potential applications. Researchers can use Ethanol, 2-(2-isothiocyanatoethoxy)- to explore new chemical reactions and develop innovative products and processes.
Used in Industrial Settings:
Ethanol, 2-(2-isothiocyanatoethoxy)is used in industrial settings for its potential applications in various industries, such as pharmaceuticals, cosmetics, and materials science. Its unique properties make it a valuable component in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 194154-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,1,5 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 194154-02:
(8*1)+(7*9)+(6*4)+(5*1)+(4*5)+(3*4)+(2*0)+(1*2)=134
134 % 10 = 4
So 194154-02-4 is a valid CAS Registry Number.
194154-02-4Relevant academic research and scientific papers
Ang, M. Trisha C.,Phan, Lam,Alshamrani, Aliyah K.,Harjani, Jitendra R.,Wang, Ruiyao,Schatte, Gabriele,Mosey, Nicholas J.,Jessop, Philip G.
, p. 7334 - 7343 (2015)
The interaction between carbon dioxide (CO2) and amidines such as 1,8-diazabicyclo[5.4.0]undecane (DBU) has been extensively studied, but the reaction of isovalent CS2 with such bases has been largely ignored, apart from a single crystallography report. Acyclic acetamidines are cleaved by CS2 at room temperature to give an isothiocyanate and a thioacetamide. Because the pathway to that cleavage involves a rotation that is difficult for cyclic amidines, the reaction of CS2 with cyclic amidines produces an entirely different product: a cyclic carbamic carboxylic trithioanhydride structure. The path to that product involves sp3 C-H activation leading to the formation of a new C-C bond at a carbon α to the central carbon of the amidine group. Alkylation and ring-opening of the cyclic carbamic carboxylic trithioanhydride has also been demonstrated under ambient conditions.
