3375-84-6 Usage
Uses
Used in Pharmaceutical Industry:
3-(2-HYDROXYPROPYL)-5-METHYL-2-OXAZOLIDINONE is used as a building block in the synthesis of various pharmaceuticals. Its antimicrobial and antibacterial properties make it a promising candidate for the development of new drugs to combat bacterial infections.
Used in Agrochemical Industry:
In the agrochemical industry, 3-(2-HYDROXYPROPYL)-5-METHYL-2-OXAZOLIDINONE is utilized as a component in the creation of agrochemicals. Its antimicrobial properties can contribute to the development of products that protect crops from bacterial diseases.
Used in Cosmetic and Personal Care Industry:
3-(2-HYDROXYPROPYL)-5-METHYL-2-OXAZOLIDINONE is used as an additive in cosmetic and personal care products. Its moisturizing and emollient properties make it suitable for inclusion in formulations that aim to hydrate and improve the skin's condition.
Check Digit Verification of cas no
The CAS Registry Mumber 3375-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3375-84:
(6*3)+(5*3)+(4*7)+(3*5)+(2*8)+(1*4)=96
96 % 10 = 6
So 3375-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO3/c1-5(9)3-8-4-6(2)11-7(8)10/h5-6,9H,3-4H2,1-2H3
3375-84-6Relevant articles and documents
Converting urea into high value-added 2-oxazolidinones under solvent-free conditions
Wang, Peixue,Li, Qinghe,Liu, Shimin,Deng, Youquan
, p. 94382 - 94386 (2016/10/21)
Zn-modified mesoporous Mg-Al nanoplates oxides were prepared by co-precipitation and further characterized and used in the synthesis of 2-oxazolidinones from urea and epoxides under solvent-free conditions. The characterization results suggested that Zn1.1Mg2.0AlO4.6, which featured more accessible active medium basic sites, were favorable for obtaining superior catalytic activity. This synthetic process is mild, convenient, simple and gives good yields up to 80%.
CLEAVAGE OF 2-AMINOBENZOTHIAZOLE IN ITS INTERACTION WITH PROPYLENE OXIDE
Mil'grom, E. G.,Kosmacheva, L. P.,Rashkes, Ya. V.,Ambartsumova, R. F.
, p. 985 - 990 (2007/10/02)
In the interaction of 2-aminobenzothiazole with propylene oxide in protic solvents, formation of the products of alkylation is accompanied by opening of the heteroring.It has been found that the nature of the solvent influences the course of the reaction.Mass spectrometry has been applied in studying the composition of the reaction mixture and the dynamics of reaction product formation.The structures of the compounds that were isolated were confirmed by physicochemical methods of investigation.
