CAS 5854-78-4

O-(1,1-Dimethylethyl)-L-threonine 1,1-dimethylethyl ester

Description:

O-(1,1-Dimethylethyl)-L-threonine 1,1-dimethylethyl ester, also known by its CAS number 5854-78-4, is an organic compound characterized by its ester functional group and the presence of a threonine amino acid derivative. This compound features a bulky tert-butyl group (1,1-dimethylethyl) attached to the threonine structure, which can influence its solubility and reactivity. Typically, such esters are used in various chemical syntheses and may serve as intermediates in the production of pharmaceuticals or agrochemicals. The presence of the amino acid moiety suggests potential biological activity, making it of interest in biochemical research. Its stability and reactivity can be affected by factors such as pH and temperature, and it may undergo hydrolysis under certain conditions. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards. Overall, this compound exemplifies the intersection of organic chemistry and biochemistry, showcasing the importance of amino acid derivatives in synthetic applications.

Formula: C₁₂H₂₅NO₃

InChI: InChI=1S/C12H25NO3/c1-8(15-11(2,3)4)9(13)10(14)16-12(5,6)7/h8-9H,13H2,1-7H3/t8-,9+/m1/s1

InChI key: InChIKey=PPDIUNOGUIAFLV-BDAKNGLRSA-N

SMILES: [C@@H]([C@@H](C(OC(C)(C)C)=O)N)(OC(C)(C)C)C

Synonyms:

• <span class="text-smallcaps">L</span>-Threonine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester
• Butyric acid, 2-amino-3-tert-butoxy-, tert-butyl ester
• Butyric acid, 2-amino-3-tert-butoxy-, tert-butyl ester, <span class="text-smallcaps">L</span>-
• H-Thr(Tbu)-Otbu
• L-threonine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester
• O-(1,1-Dimethylethyl)-<span class="text-smallcaps">L</span>-threonine 1,1-dimethylethyl ester
• O-tert-Butyl-<span class="text-smallcaps">L</span>-threonine tert-butyl ester
• O-tert-Butyl-L-threonine tert-Butyl Ester
• O-tert-Butylthreonine tert-butyl ester
• tert-Butyl O-tert-butyl-L-threoninate
• Butyric acid, 2-amino-3-tert-butoxy-, tert-butyl ester, L-

O-tert-Butyl-L-threonine tert-Butyl Ester

CAS: 5854-78-4

Formula: C₁₂H₂₅NO₃

Purity: >96.0%(T)

Color and Shape: Colorless to Red to Green clear liquid

Molecular weight: 231.34

Ref: 3B-B3340

H-Thr(tBu)-OtBu

CAS: 5854-78-4

Formula: C₁₂H₂₅NO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 231.3318

Ref: IN-DA003TI4

O-Tert-Butyl-L-Threonine Tert-Butyl Ester

CAS: 5854-78-4

O-Tert-Butyl-L-Threonine Tert-Butyl Ester

Purity: 98%

Molecular weight: 231.33g/mol

Ref: 54-OR1014561

(2S,3R)-tert-Butyl 2-amino-3-(tert-butoxy)butanoate

CAS: 5854-78-4

Formula: C₁₂H₂₅NO₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 231.336

Ref: 10-F211467

O-tert-Butyl-L-threonine tert-butyl ester

CAS: 5854-78-4

O-tert-Butyl-L-threonine tert-butyl ester is a bactericidal antibiotic that belongs to the class of galacturonic acid. It inhibits bacterial growth by binding to the enzyme transpeptidase, which is crucial in crosslinking peptidoglycan chains. This antibiotic has been shown to have antibacterial activity against bacteria such as Staphylococcus aureus and Streptococcus pyogenes. O-tert-Butyl-L-threonine tert-butyl ester has been used for the production of lactic acid from glucose in bioreactors. The lactic acid can be used for the production of polymers, and the fermentation process can be done using either yeast or bacteria, such as pastoris or trifluoroacetic acid. The reaction time is typically between 4 and 6 hours, at a temperature of 25 °C with an acid catalyst such as hydrochloric acid

Formula: C₁₂H₂₅NO₃

Purity: Min. 98%

Color and Shape: Slightly Yellow Clear Liquid

Molecular weight: 231.33 g/mol

Ref: 3D-FT46578