CAS 30992-29-1

N-[(1,1-Dimetiletoxicabonil)-2-metilalanina

Descrizione:

N-[(1,1-Dimetiletoxicabonil)-2-metilalanina, con il numero CAS 30992-29-1, è un derivato di aminoacido caratterizzato dalla presenza di un gruppo carbonilico e di un gruppo protettivo dimetiletossile ingombrante. Questo composto tipicamente mostra proprietà associate agli aminoacidi, come la capacità di formare legami idrogeno e partecipare a varie reazioni chimiche grazie ai suoi gruppi funzionali. Il gruppo dimetiletossile migliora la sua lipofilia, il che può influenzare la sua solubilità in solventi organici rispetto all'acqua. Inoltre, la presenza del gruppo metile sul carbonio alfa contribuisce alle sue proprietà steriche, potenzialmente influenzando la sua reattività e interazioni nei sistemi biologici. Questo composto è spesso utilizzato nella sintesi di peptidi e in altre applicazioni di sintesi organica, dove la protezione dei gruppi funzionali è cruciale per reazioni selettive. La sua stabilità e reattività possono essere influenzate da fattori ambientali come pH e temperatura, rendendo importante considerare queste condizioni durante la manipolazione e la sperimentazione.

Formula: C₉H₁₇NO₄

InChI: InChI=1S/C9H17NO4/c1-8(2,3)14-7(13)10-9(4,5)6(11)12/h1-5H3,(H,10,13)(H,11,12)

InChI key: InChIKey=MFNXWZGIFWJHMI-UHFFFAOYSA-N

SMILES: C(NC(C(O)=O)(C)C)(OC(C)(C)C)=O

Sinonimi:

• 2-(((tert-Butoxy)carbonyl)amino)-2-methylpropanoic acid
• 2-(Boc-amino)isobutyric acid
• 2-(tert-Butoxycarbonylamino)isobutanoic acid
• 2-(tert-Butoxycarbonylamino)isobutyric acid
• 2-(tert-Butoxycarboxylamino)-2-methylpropanoic acid
• 2-(tert-Butyloxycarbonylamino)isobutanoic acid
• 2-Methyl-2-((t-butyloxycarbonyl)amino)propionic acid
• 2-Methyl-2-[(2-Methylpropan-2-Yl)Oxycarbonylamino]Propanoic Acid
• 2-[(Tert-Butoxycarbonyl)Amino]-2-Methylpropanoate
• 2-[(tert-Butoxycarbonyl)amino]-2-methylpropionic acid
• Alanine, N-[(1,1-dimethylethoxy)carbonyl]-2-methyl-
• Alanine, N-carboxy-2-methyl-, N-tert-butyl ester
• BOC-alpha-Methylalanine
• Boc-2-aminoisobutyric acid
• Boc-2-methylalanine
• Boc-Aib-OH
• Boc-aminoisobutyric acid
• Boc-α-methylalanine
• N-(tert-Butoxycarbonyl)-2,2-dimethylglycine
• N-(tert-Butoxycarbonyl)-2-methylalanine
• N-(tert-Butoxycarbonyl)-α-methylalanine
• N-(tert-Butyloxycarbonyl)-2-aminoisobutyric acid
• N-BOC-α-methylalanine
• N-Boc-2,2-dimethylglycine
• N-Boc-2-amino-2-methylpropanoic acid
• N-Boc-2-aminoisobutyric acid
• N-Boc-2-methylalanine
• N-Boc-α,α-dimethylglycine
• N-[(1,1-Dimethylethoxy)carbonyl]-2-methylalanine
• N-tert-Butoxycarbonyl-2-aminoisobutyric acid
• N-tert-Butoxycarbonyl-α-aminoisobutyric acid
• α-(Bocamino)isobutyric acid

N-Boc-2-aminoisobutyric acid, 98+%

CAS: 30992-29-1

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 Sci

Formula: C₉H₁₆NO₄

Purezza: 98+%

Colore e forma: White, Crystals or powder or crystalline powder

Peso molecolare: 202.23

Ref: 02-L19484

Boc-Aib-OH

CAS: 30992-29-1

Bachem ID: 4010082.

Formula: C₉H₁₇NO₄

Purezza: > 99%

Colore e forma: White

Peso molecolare: 203.24

Ref: 01-4010082

N-(tert-Butyloxycarbonyl)-2-aminoisobutyric acid

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 203.2356

Ref: IN-DA003OFR

Boc-Aib-OH

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Peso molecolare: 203.24

Ref: 7W-GM2007

α-(Boc-Amino)Isobutyric Acid

CAS: 30992-29-1

α-(Boc-Amino)Isobutyric Acid

Purezza: 98%

Peso molecolare: 203.24g/mol

Ref: 54-OR1015473

2-(tert-Butoxycarbonylamino)isobutyric Acid

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Purezza: >98.0%(GC)(T)

Colore e forma: White to Almost white powder to crystal

Peso molecolare: 203.24

Ref: 3B-B3323

Boc-a-aminoisobutyric acid

CAS: 30992-29-1

Boc-a-aminoisobutyric acid is a tetrapeptide pyridinium amine with a helical structure. It is synthesized by the acid conjugate of 2-aminobutyric acid and tetrazole in liquid phase, then converted to its solid form by the addition of BocCl. The synthesis of Boc-a-aminoisobutyric acid is achieved through the use of solid-phase synthesis as well as 2-aminobutyric acid. This drug has been shown to be a potent secretagogue that stimulates gastrin release in vitro and in vivo. It may also have clinical uses for gastrinomas, Zollinger Ellison syndrome, and others. Boc-a-aminoisobutyric acid's ability to stimulate secretion of gastrin is attributed to its intramolecular hydrogen bond with the amide group.

Formula: C₉H₁₇NO₄

Purezza: Min. 98 Area-%

Colore e forma: White Off-White Powder

Peso molecolare: 203.24 g/mol

Ref: 3D-FB47799

Boc-2-aminoisobutyric acid

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Purezza: 95%

Colore e forma: Solid, White crystalline

Peso molecolare: 203.238

Ref: 10-F075038

Boc-α-Methylalanine

Prodotto controllato

CAS: 30992-29-1

Applications Boc-α-Methylalanine is used as a catalyst in the preparation of 2-benzopyranone derivatives (isocoumarin) as well as arylbenzeneacetic acids.
References Lu, Y. et al.: Chem. Sci., 2, 967 (2011); Engle, K. et al.: JK. Am. Chem. Soc., 133, 18183 (2011);

Formula: C₉H₁₇NO₄

Colore e forma: Neat

Peso molecolare: 203.24

Ref: TR-B656940