138629-30-8 Usage
Description
(2R)-2-[[[(1,1-DIMETHYLETHYL)DIPHENYLSILYL]OXY]METHYL]-5-OXO-1-PYRROLIDINECARBOXYLATE-1,1-DIMETHYLETHYL ESTER is a complex organic compound characterized by a pyrrolidine ring, a carboxylate ester, and a diphenylsilyl group. It is derived from 1,1-dimethylethyl diphenylsilyloxy acetic acid and features a methyl group and a 5-oxo functional group. The presence of ester and carboxylate groups suggests that this compound may exhibit lipophilic properties, making it a candidate for applications in the pharmaceutical or materials industries. The diphenylsilyl group could also indicate potential uses in organic synthesis or as a protectant for sensitive functional groups.
Uses
Used in Pharmaceutical Industry:
(2R)-2-[[[(1,1-DIMETHYLETHYL)DIPHENYLSILYL]OXY]METHYL]-5-OXO-1-PYRROLIDINECARBOXYLATE-1,1-DIMETHYLETHYL ESTER is used as a pharmaceutical intermediate for the synthesis of various drugs due to its complex structure and functional groups. Its lipophilic nature allows for improved drug delivery and bioavailability.
Used in Materials Industry:
In the materials industry, (2R)-2-[[[(1,1-DIMETHYLETHYL)DIPHENYLSILYL]OXY]METHYL]-5-OXO-1-PYRROLIDINECARBOXYLATE-1,1-DIMETHYLETHYL ESTER is used as a component in the development of advanced materials, such as polymers or coatings, that require specific chemical properties conferred by its functional groups.
Used in Organic Synthesis:
(2R)-2-[[[(1,1-DIMETHYLETHYL)DIPHENYLSILYL]OXY]METHYL]-5-OXO-1-PYRROLIDINECARBOXYLATE-1,1-DIMETHYLETHYL ESTER serves as a reactant or building block in organic synthesis, where its unique structure and functional groups can be utilized to create novel compounds with specific properties.
Used as a Protectant in Sensitive Reactions:
The diphenylsilyl group present in (2R)-2-[[[(1,1-DIMETHYLETHYL)DIPHENYLSILYL]OXY]METHYL]-5-OXO-1-PYRROLIDINECARBOXYLATE-1,1-DIMETHYLETHYL ESTER allows it to be used as a protectant for sensitive functional groups during chemical reactions, preventing unwanted side reactions and improving the yield of desired products.
Check Digit Verification of cas no
The CAS Registry Mumber 138629-30-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138629-30:
(8*1)+(7*3)+(6*8)+(5*6)+(4*2)+(3*9)+(2*3)+(1*0)=148
148 % 10 = 8
So 138629-30-8 is a valid CAS Registry Number.
138629-30-8Relevant articles and documents
COMPOUNDS TARGETING RNA-BINDING PROTEINS OR RNA-MODIFYING PROTEINS
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Page/Page column 242; 243, (2021/09/11)
The invention relates to a compound represented by Formula (I): or a pharmaceutically acceptable salt thereof, compositions comprising the same and methods of preparing and using the same. The variables are described herein.
A Unified Strategy for the Synthesis of Difluoromethyl- And Vinylfluoride-Containing Scaffolds
Duchemin, Nicolas,Buccafusca, Roberto,Daumas, Marc,Ferey, Vincent,Arseniyadis, Stellios
supporting information, p. 8205 - 8210 (2019/10/16)
Here, we report a general method for the synthesis of quaternary and tertiary difluoromethylated compounds and their vinylfluoride analogues. The strategy, which relies on a two-step sequence featuring a C-selective electrophilic difluoromethylation and either a palladium-catalyzed decarboxylative protonation or a Krapcho decarboxylation, is practical, scalable, and high yielding. Considering the generality of the method and the attractive properties offered by the difluoromethyl group, this approach provides a valuable tool for late-stage functionalization and drug development.
INDOLE DERIVATIVES AS EFFLUX PUMP INHIBITORS
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Page/Page column 80, (2018/09/28)
Disclosed herein are compounds of formula (I): and salts thereof. Also disclosed are compositions comprising compounds of formula I and compounds of formula I for use in treating or preventing bacterial infections.
