134038-74-7 Usage
Description
3-Oxazolidinecarboxylic acid, 5-forMyl-2,2-diMethyl-, phenylMethyl ester, (5S)is a chiral phenylMethyl ester derivative of 3-Oxazolidinecarboxylic acid, 5-forMyl-2,2-diMethyl-. 3-Oxazolidinecarboxylic acid, 5-forMyl-2,2-diMethyl-, phenylMethyl ester, (5S)is characterized by its (5S)configuration, which is crucial for its potential applications in various fields. It is commonly utilized in organic synthesis and pharmaceutical research, and may hold promise for the development of new drugs or the production of fine chemicals. Due to its reactivity and potential hazards, it is essential to handle this chemical with care and adhere to proper safety protocols in laboratory settings.
Uses
Used in Organic Synthesis:
3-Oxazolidinecarboxylic acid, 5-forMyl-2,2-diMethyl-, phenylMethyl ester, (5S)is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure and chiral configuration make it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-Oxazolidinecarboxylic acid, 5-forMyl-2,2-diMethyl-, phenylMethyl ester, (5S)is used as a starting material or a synthetic intermediate for the development of new drugs. Its chiral (5S)configuration allows for the creation of enantiomerically pure compounds, which is essential for the discovery of drugs with improved efficacy and reduced side effects.
Used in the Production of Fine Chemicals:
3-Oxazolidinecarboxylic acid, 5-forMyl-2,2-diMethyl-, phenylMethyl ester, (5S)is also utilized in the production of fine chemicals, which are high-purity chemicals used in various applications such as fragrances, flavors, dyes, and other specialty products. Its unique structure and chiral properties contribute to the development of novel and high-quality fine chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 134038-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,3 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134038-74:
(8*1)+(7*3)+(6*4)+(5*0)+(4*3)+(3*8)+(2*7)+(1*4)=107
107 % 10 = 7
So 134038-74-7 is a valid CAS Registry Number.
134038-74-7Relevant articles and documents
Organocatalytic syn-aldol reactions of hydroxy ketones with (S)-isoserinal: Asymmetric synthesis of 6-deoxy-1,5-iminohexitols and related compounds
Nicolas, Cyril,Pluta, Roman,Pasternak-Suder, Monika,Martin, Olivier R.,Mlynarski, Jacek
, p. 1296 - 1305 (2013/04/10)
An improved and convenient preparation of protected (S)-isoserinal on a large scale is reported. This key intermediate was reacted through organocatalyzed aldol reaction or Wittig based chain extension and functionalization to give enantiopure 1,5,6-trideoxy-1,5-imino-hexitols such as 10a (L-manno) and 10b (D-gluco). These two compounds are of interest as glycosidase inhibitors. The elaborated organocatalytic process includes diastereoselective syn aldol reaction of (S)-isoserinal hydrate and hydroxyacetone or 1-hydroxy-2-octanone and is promoted by various amino acid-based catalysts. Diastereoselectivities of up to 8:1 were achieved, thus establishing a new, efficient synthetic route to these important carbohydrate mimics. A novel protocol for the preparation of 1,5,6-trideoxy-1,5-imino-L- mannitol and 1,5,6-trideoxy-1,5-imino-D-glucitol is reported. The key steps include organocatalyzed syn-selective direct aldol reaction of hydroxyacetone and CBz-protected isoserinal hydrate, followed by reductive amination/ cyclization. Copyright
Substituted imidazole derivatives
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Page/Page column 37, (2008/06/13)
The present invention relates to new substituted imidazole compounds and pharmaceutically acceptable salts, esters or prodrugs thereof, compositions of the new compounds together with pharmaceutically acceptable carriers, and uses of the new compounds. The compounds of the invention have the following general formula:
The Synthesis of Biphenomycin B
Schmidt, Ulrich,Meyer, Regina,Leitenberger, Volker,Lieberknecht, Albrecht,Griesser, Helmut
, p. 275 - 277 (2007/10/02)
Biphenomycin B, a highly potent antibiotic against Gram-negative, β-lactam-resistant bacteria, which was previously isolated from culture filtrates of Streptomyces griseorubiginosus No. 43708, has now been synthesized.
