21055-41-4 Usage
Uses
Used in Pharmaceutical Applications:
Methyl L-2-isothiocyanato-3-methylbutyrate is utilized as a pharmaceutical agent for its potential anti-cancer properties, targeting the inhibition of cancer cell growth. Its unique biological activities and potential therapeutic benefits make it a valuable compound in the development of new cancer treatments.
Used in Research:
In the research field, Methyl L-2-isothiocyanato-3-methylbutyrate serves as a subject of study for its biological activities and potential applications in medicine. Scientists are exploring its mechanisms of action and how it can be harnessed for therapeutic purposes.
Used in Antimicrobial Applications:
Methyl L-2-isothiocyanato-3-methylbutyrate is employed as an antimicrobial agent, leveraging its natural properties to combat various microorganisms. This application can be particularly useful in the development of new antibiotics or disinfectants.
Used in Insecticidal Applications:
As an insecticidal agent, Methyl L-2-isothiocyanato-3-methylbutyrate is used to control and manage insect populations. Its insecticidal properties can be integrated into pest control strategies in agriculture and other industries to protect crops and reduce the reliance on chemical pesticides.
Check Digit Verification of cas no
The CAS Registry Mumber 21055-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,5 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21055-41:
(7*2)+(6*1)+(5*0)+(4*5)+(3*5)+(2*4)+(1*1)=64
64 % 10 = 4
So 21055-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO2S/c1-5(2)6(8-4-11)7(9)10-3/h5-6H,1-3H3/t6-/m0/s1
21055-41-4Relevant articles and documents
Na2S2O8-mediated efficient synthesis of isothiocyanates from primary amines in water
Fu, Zhicheng,Yuan, Wenhao,Chen, Ning,Yang, Zhanhui,Xu, Jiaxi
supporting information, p. 4484 - 4491 (2018/10/17)
We have developed two green, practical, and efficient procedures, including a one-pot one, to synthesize isothiocyanates from amines and carbon disulfide via desulfurization with sodium persulfate. Water is used as the solvent. Basic conditions are necessary for good chemoselectivity for isothiocyanates. Structurally diverse linear and branched alkyl amines and aryl amines are readily converted to isothiocyanates by the two procedures in satisfactory yields. Halogens, benzylic C-H bonds, methylthio, nitro, ester, alkenyl, electron-rich or -deficient (hetero)aryls, acetylenyl, and even phenolic and alcoholic hydroxyls are well tolerated. The one-pot procedure in water can also be used to realize the preparation of chiral isothiocyanates from chiral amines, and the modification of bioactive structures with free amino groups. In large-scale preparation, simple and practical purification procedures independent of column chromatography are developed.
Novel derivatives of benzimidazole and imidazo-pyridine and their use as medicaments
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Page/Page column 12-14, (2008/06/13)
A compound of the formula wherein the substituents are as defined in the specification and pharmaceutical salts thereof having a good affinity for sub-types of melanocortin receptors making them useful for treating diseases in which such receptors are included such as pain, inflammatory conditions, etc.
