
CAS 2026-48-4: 1-Butanolo, 2-ammino-3-metil-, (2S)-
Descrizione:
1-Butanolo, 2-ammino-3-metil-, (2S)-, noto anche come (S)-2-amino-3-metil-1-butanolo, è un composto organico caratterizzato dalla sua struttura di aminoalcol. Presenta uno scheletro di butanolo con un gruppo amminico (-NH2) e un gruppo metile (-CH3) attaccati al secondo e terzo atomo di carbonio, rispettivamente. Questo composto è una molecola chirale, con la designazione (2S) che indica la sua stereochimica specifica. È tipicamente un liquido incolore a giallo pallido con un odore caratteristico ed è solubile in acqua grazie alla presenza del gruppo idrossile (-OH). La presenza di entrambi i gruppi funzionali, amminico e idrossile, consente di partecipare a legami idrogeno, influenzando le sue proprietà fisiche e reattività. 1-Butanolo, 2-ammino-3-metil-, (2S)- è spesso utilizzato in varie sintesi chimiche e può fungere da intermedio nella produzione di prodotti farmaceutici o agrochimici. La sua attività biologica e le potenziali applicazioni in chimica medicinale sono aree di ricerca in corso.
Formula:C5H13NO
InChI:InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1
InChI key:InChIKey=NWYYWIJOWOLJNR-RXMQYKEDSA-N
SMILES:[C@H](C(C)C)(CO)N
Sinonimi:- (+)-(S)-Valinol
- (+)-2-Amino-3-methyl-1-butanol
- (+)-Valinol
- (2S)-1-Hydroxy-3-methylbutan-2-amine
- (2S)-2-Amino-3-methyl-1-butanol
- (2S)-Valinol
- (S)-(+)-2-Amino-3-methyl-1-butanol
- (S)-2-Amino-3-methylbutanol
- 1-Butanol, 2-amino-3-methyl-, (S)-
- 1-Butanol, 2-amino-3-methyl-, <span class="text-smallcaps">L</span>-
- 1-Butanol, 2-amino-3-methyl-, L-
- Vedi altri sinonimi
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11 prodotti.
(S)-(+)-2-Amino-3-methyl-1-butanol, 96%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C5H13NOPurezza:96%Colore e forma:Liquid after melting or solid, Clear colorless to white to light yellowPeso molecolare:103.17L-Valinol
CAS:M03447 - L-ValinolFormula:C5H13NOPurezza:95%Colore e forma:LiquidPeso molecolare:103.16500091552734L-Valinol
CAS:Prodotto controllatoApplications L-Valinol is used as a reagent in the synthesis of simple 1,3-thiazolidine-2-thione derivatives which can exhibit fungicidal activity. L-Valinol is also used as a reagent in the synthesis of small-molecule inhibitors of MDM2-p53 protein-protein interaction (MDM2 inhibitors) in clinical trials for the treatment of cancer. References Chen, N., et al.: Phosphorus Sulfur, 190, 112 (2015); Zhao, Y., et al.: J. Med. Chem., 58, 1038 (2015)Formula:C5H13NOColore e forma:WhitePeso molecolare:103.163L-(+)-Valinol, 97%
CAS:L-(+)-Valinol reacts with aldehydes and nitriles to form imines and oxazolines, respectively, for asymmetric synthesis. It is also used for preparation of 4-isopropyloxazolidinones, employed in stereocontrolled aldol and alkylation reactions, synthesis of chiral 2-thiazolidinethiones for aldol reactions, asymmetric alkylation of condensation product with keto acids, asymmetric reactions of its amidines and imines and oxidation of N-protected derivative to the aldehyde. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C5H13NOPurezza:97%Colore e forma:Colourless/white to yellow, liquid/low melting solidPeso molecolare:103.17L-Valinol
CAS:Formula:C5H13NOPurezza:>97.0%(GC)(T)Colore e forma:White or Colorless to Light orange to Yellow powder to lump to clear liquidPeso molecolare:103.17(S)-(+)-2-Amino-3-methyl-1-butanol
CAS:(S)-(+)-2-Amino-3-methyl-1-butanolFormula:C5H13NOPurezza:97%Colore e forma: colourless to light yellow crystalline solidPeso molecolare:103.16g/molL-Valinol
CAS:L-Valinol is a model system that is used to study the reaction of aziridines with oxygen nucleophiles. It has been shown that this reaction proceeds through the formation of an intermediate, hydrogen tartrate, followed by a second step with nitrogen atoms as the nucleophile and alcohol residue as the substrate. The use of L-valinol in asymmetric synthesis was also demonstrated. In this process, amides were obtained with high enantioselectivity by reacting L-valinol with amines in acidic conditions. This synthetic pathway was found to be synergic with other reactions, such as nitroolefination and benzoylation.Formula:C5H13NOPurezza:Min. 95%Colore e forma:Solidified MassPeso molecolare:103.16 g/molL-Valinol
CAS:Formula:C5H13NOPurezza:≥ 97.0%Colore e forma:Colourless to white or pale yellow solid, crystals or liquidPeso molecolare:103.17