CAS 90776-58-2

(R)-2-[(3S,4S)-3-[(R)-1-(tert-Butyldimethylsilyloxy)ethyl]-2-oxoazetidin-4-yl]propionic acid

Description:

The chemical substance known as (R)-2-[(3S,4S)-3-[(R)-1-(tert-Butyldimethylsilyloxy)ethyl]-2-oxoazetidin-4-yl]propionic acid, with the CAS number 90776-58-2, is a chiral compound featuring a complex structure that includes an azetidine ring and a propionic acid moiety. Its stereochemistry is significant, as it contains multiple chiral centers, which can influence its biological activity and interactions. The presence of the tert-butyldimethylsilyloxy group suggests that this compound may be used in synthetic organic chemistry, particularly in protecting group strategies or as an intermediate in the synthesis of more complex molecules. The azetidine ring contributes to the compound's rigidity and may affect its pharmacokinetic properties. Additionally, the propionic acid component indicates potential applications in medicinal chemistry, possibly as a pharmaceutical agent. Overall, the compound's unique structural features and stereochemistry make it of interest in various fields, including drug development and organic synthesis.

Formula: C₁₄H₂₇NO₄Si

InChI: InChI=1S/C14H27NO4Si/c1-8(13(17)18)11-10(12(16)15-11)9(2)19-20(6,7)14(3,4)5/h8-11H,1-7H3,(H,15,16)(H,17,18)/t8-,9-,10-,11-/m1/s1

InChI key: InChIKey=NNANGMFTFSNDLW-GWOFURMSSA-N

SMILES: [C@@H](C(O)=O)(C)[C@@]1([C@@]([C@H](O[Si](C(C)(C)C)(C)C)C)(C(=O)N1)[H])[H]

Synonyms:

• (2R)-2-{(2S,3S)-3-[(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}ethyl]-4-oxoazetidin-2-yl}propanoic acid
• (3S 4S)-3-[(R)-1-(T-Butyldimethylsilyloxy)Ethyl]-4-[(R)-1-Carboxyethyl]-2-Azetidinone
• (3S,4S)-3-[(1R)-1-[(tert-Butyldimethylsilyl)oxy]ethyl]-4-((1R)-1-carboxyethyl)azetidin-2-one
• (3S,4S)-3-[(R)-(Butyldimethylsilyloxy)Ethyl]-4-[(R)-Carboxyethyl]-2-Azetidinone
• (3S,4S)-3-[(R)-1-(Tert-Butyldimethylsiloxy)Ethyl]-4-[(R)-1-Carboxyethyl]-2-Azetidinone
• (3S,4S)-3-[(R)-1-(Tert-Butyldimethylsilyloxy)Ethyl]-4-[(R)-1-Carboxyethyl]-2-Azetidinone
• (3S,4S)-4-[(R)-1-carboxy-ethyl]-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone
• (3S,4S)-4-[(R)-1-carboxyethyl]-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone
• (R)-2-((2S,3S)-3-((R)-1-(Tert-Butyldimethylsilyloxy)Ethyl)-4-Oxoazetidin-2-Yl)Propanoic Acid
• (R)-2-[(3S,4S)-3-[(R)-1-(tert-Butyldimethylsilyloxy)ethyl]-2-oxoazetidin-4-yl]propionic acid
• (αR,2S,3S)-3-[(1R)-1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]-α-methyl-4-oxo-2-azetidineacetic acid
• 1-Bma
• 2-Azetidineacetic acid, 3-[(1R)-1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl]-α-methyl-4-oxo-, (αR,2S,3S)-
• 2-Azetidineacetic acid, 3-[1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl]-α-methyl-4-oxo-, [2S-[2α(S*),3β(S*)]]-
• 4-BMA(for Meropenem)
• 4-Bma
• 4Bma
• Side Chain For Imipenem
• [2R-[2α(R*),3β(R*)] ]-3-[1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl]-α-methl-4-oxo-2-azetidineacetic acid

(3S,4S)-4-[(R)-1-carboxyethyl]-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone

CAS: 90776-58-2

Formula: C₁₄H₂₇NO₄Si

Purity: 97%

Color and Shape: Solid

Molecular weight: 301.4540

Ref: IN-DA003BTJ

(R)-2-((2S,3S)-3-((R)-1-((Tert-Butyldimethylsilyl)Oxy)Ethyl)-4-Oxoazetidin-2-Yl)Propanoic Acid

CAS: 90776-58-2

(R)-2-((2S,3S)-3-((R)-1-((Tert-Butyldimethylsilyl)Oxy)Ethyl)-4-Oxoazetidin-2-Yl)Propanoic Acid

Purity: 95%

Molecular weight: 301.45g/mol

Ref: 54-OR1008440

(3S 4S)-3-[ (R)-1-(T-Butyldimethylsilyloxy)ethyl]-4[(R)-1-carboxyethyl]-2-azetidinone

CAS: 90776-58-2

S03379 - (3S 4S)-3-[ (R)-1-(T-Butyldimethylsilyloxy)ethyl]-4[(R)-1-carboxyethyl]-2-azetidinone

Formula: C₁₄H₂₇NO₄Si

Purity: 97%

Color and Shape: Solid

Molecular weight: 301.458

Ref: 10-S03379

(3S,4S)-3-((R)-(tert-Butyldimethyl-silyloxy)ethyl)-4((R)-carboxyethyl)-2-azetidinone

CAS: 90776-58-2

(3S,4S)-3-((R)-(tert-Butyldimethyl-silyloxy)ethyl)-4((R)-carboxyethyl)-2-azetidinone (SBET) is a propionylated carbapenem antibiotic. It is an analog of ertapenem, a carbapenem antibiotic that has been developed for the treatment of multidrug resistant Gram-negative bacteria. SBET has been shown to have stereospecificity in vitro studies and to be metabolized by organic acids. The reaction yields are dependent on the solvents used. The functional groups on SBET are important for its activity as a carbapenem antibiotic.

Formula: C₁₄H₂₇NO₄Si

Purity: Min. 95%

Molecular weight: 301.45 g/mol

Ref: 3D-FB149807