4270-00-2 Usage
Uses
Used in Organic Synthesis:
Carbamimidothioic acid, bromide, pentyl ester is used as an intermediate in the synthesis of various organic compounds for [application reason]. Its unique structure and functional groups allow it to participate in a wide range of chemical reactions, making it a valuable building block in the development of new molecules and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, carbamimidothioic acid, bromide, pentyl ester is used as a starting material for the development of new drugs and drug candidates for [application reason]. Its ability to form various chemical bonds and its reactivity make it a promising candidate for the creation of novel therapeutic agents.
Used in Chemical Research:
Carbamimidothioic acid, bromide, pentyl ester is also used in chemical research as a model compound to study the properties and reactions of similar compounds for [application reason]. Its unique structure and reactivity provide valuable insights into the behavior of related compounds and contribute to the advancement of chemical knowledge.
Used in Agrochemical Industry:
In the agrochemical industry, carbamimidothioic acid, bromide, pentyl ester is used as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides, for [application reason]. Its versatility in chemical reactions allows for the development of effective and targeted agrochemical products.
Overall, carbamimidothioic acid, bromide, pentyl ester is a versatile and complex chemical compound with potential applications in various industries, including organic synthesis, pharmaceuticals, chemical research, and agrochemicals. Its unique structure and reactivity make it a valuable asset in the development of new molecules, materials, and products.
Check Digit Verification of cas no
The CAS Registry Mumber 4270-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4270-00:
(6*4)+(5*2)+(4*7)+(3*0)+(2*0)+(1*0)=62
62 % 10 = 2
So 4270-00-2 is a valid CAS Registry Number.
4270-00-2Relevant academic research and scientific papers
Synthesis of sulfides by reactions of 1,1-dichloro-2-chloro- methylcyclopropane with S-nucleophiles
Mikhed'kina,Nedel'ko,Prezhdo
, p. 370 - 375 (2007/10/03)
1,1-Dichloro-2-chloromethylcyclopropane reacts with thiolates to give 2,2-dichlorocyclopropylmethyl sulfides via replacement of the side-chain chlorine atom. The resulting sulfides are readily oxidized to the corresponding sulfones.
Organic-Soluble Lanthanide Nuclear Magnetic Resonance Shift Reagents for Sulfonium and Isothiuronium Salts
Wenzel, Thomas J.,Zaia, Joseph
, p. 562 - 567 (2007/10/02)
Lanthanide complexes of the formula 4>- (fod, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione) are effective organic-soluble nuclear magnetic resonance shift reagents for sulfonium and isothiuronium salts.The shift reagent is formed in solution from Ln(fod)3 and Ag(fod) or K(fod).The selection of Ag(fod) or K(fod) in forming the shift reagent is dependent on the anion of the organic salt.Ag(fod) is more effective with halide salts, whereas K(fod) is preferred with tetrafluoroborate salts.Resolution of diastereotopic hydrogen atoms was observed in the shifted spectra of certain substrates.Enantiomeric resolution was obtained in the spectrum of sec-butylisothiuronium chloride with a chiral shift reagent.The reagents can be employed in solvents such as chloroform and benzene.
SYNTHESIS OF MONO(ALKYLTHIO)-SUBSTITUTED KETONES
Sabirov, S. S.,Gnevasheva, L. M.,Ismailov, M. I.,Isobaev, M. D.
, p. 1239 - 1243 (2007/10/02)
In the reaction of 2-propanone in the presence of sodium bicarbonate with a mixture of formaldehyde and the corresponding alkaline hydrolyzates of S-alkylthiuronium salts (thioalcoholates) β-keto sulfides (1-alkylthio-3-butanones) were obtained.Ketalization of the products with glycerol gave the cyclic derivatives alkylthio-1,3-dioxolanes.
