14366-33-7 Usage
Description
[(2-phenylhydrazino)carbonothioyl]sulfanylacetic acid is a complex organic molecule that features a phenylhydrazine group, a carbonothioyl functional group, and an acetic acid moiety. This unique structure endows the compound with a range of chemical properties and potential biological activities, making it a valuable asset in the fields of organic synthesis and pharmaceutical research.
Uses
Used in Organic Synthesis:
[(2-phenylhydrazino)carbonothioyl]sulfanylacetic acid is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of new compounds with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [(2-phenylhydrazino)carbonothioyl]sulfanylacetic acid is used as a key component in the development of new drugs. Its unique structure and chemical properties allow it to be a promising candidate for the creation of novel therapeutic agents.
Used in the Study of Organic Reactions:
[(2-phenylhydrazino)carbonothioyl]sulfanylacetic acid is also utilized in academic and research settings to study organic reactions and understand the underlying mechanisms involved. This knowledge can be applied to improve existing synthetic methods or develop new ones, ultimately contributing to the advancement of chemical science.
Overall, [(2-phenylhydrazino)carbonothioyl]sulfanylacetic acid is a versatile compound with potential applications in various fields of chemistry and medicine, including organic synthesis, pharmaceutical research, and the study of organic reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 14366-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,6 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14366-33:
(7*1)+(6*4)+(5*3)+(4*6)+(3*6)+(2*3)+(1*3)=97
97 % 10 = 7
So 14366-33-7 is a valid CAS Registry Number.
14366-33-7Relevant articles and documents
RING-CHAIN AND RING-LINEAR-RING TAUTOMERISM IN THIOCARBONOHYDRAZONES
Alekseev, V. V.,Zelenin, K. N.,Terent'ev, P. B.,Lashin, V. V.,Khorseeva, L. A.,Bulakhov, G. A.
, p. 491 - 501 (2007/10/02)
The structure of the thiocarbonohydrazones of monocarbonyl compounds was studied by 1H and 13C NMR spectroscopy in solutions and by mass spectrometry in the gas phase. In solutions, irrespective of the substitution in the aromatic ring and in the hydrazine fragment, the thiocarbonohydrazones of aromatic aldehydes exist in the linear form, whereas the 2- and 5-substituted thiocarbonohydrazones of ketones are susceptible to ring-chain tautomerism: Thiocarbonohydrazone - 4-amino-1,2,4-triazolidine-3-thione. Those not having substituents at the nitrogen atoms are susceptible to ring-linear-ring equilibria: Hexahydro-1,2,4,5-tetrazine-3-thione - thiocarbonohydrazone - 4-amino-1,2,4-triazolidine-3-thione. In the gas phase under conditions of high vacuum, according to the mass spectra, the coexistence of four tautomeric forms (linear, tetrazine, triazolidine, and 2-hydrazino-1,3,4-thiadiazolidine) is possible in individual cases.
