CAS 30992-29-1

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

Descripción:

N-[(1,1-Dimetiletoxicarbonil)-2-metilalanina, con el número CAS 30992-29-1, es un derivado de aminoácido caracterizado por la presencia de un grupo carbonilo y un grupo protector de dimetiletoxilo voluminoso. Este compuesto típicamente exhibe propiedades asociadas con los aminoácidos, como la capacidad de formar enlaces de hidrógeno y participar en diversas reacciones químicas debido a sus grupos funcionales. El grupo dimetiletoxilo mejora su lipofilia, lo que puede influir en su solubilidad en disolventes orgánicos en comparación con el agua. Además, la presencia del grupo metilo en el carbono alfa contribuye a sus propiedades estéricas, lo que puede afectar su reactividad e interacciones en sistemas biológicos. Este compuesto se utiliza a menudo en la síntesis de péptidos y otras aplicaciones de síntesis orgánica, donde la protección de grupos funcionales es crucial para reacciones selectivas. Su estabilidad y reactividad pueden verse influenciadas por factores ambientales como el pH y la temperatura, lo que hace importante considerar estas condiciones durante el manejo y la experimentación.

Fórmula: 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)

Clave InChI: InChIKey=MFNXWZGIFWJHMI-UHFFFAOYSA-N

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

Sinónimos:

• 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

Fórmula: C₉H₁₆NO₄

Pureza: 98+%

Forma y color: White, Crystals or powder or crystalline powder

Peso molecular: 202.23

Ref: 02-L19484

Boc-Aib-OH

CAS: 30992-29-1

Bachem ID: 4010082.

Fórmula: C₉H₁₇NO₄

Pureza: > 99%

Forma y color: White

Peso molecular: 203.24

Ref: 01-4010082

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

CAS: 30992-29-1

Fórmula: C₉H₁₇NO₄

Pureza: 97%

Forma y color: Solid

Peso molecular: 203.2356

Ref: IN-DA003OFR

Boc-Aib-OH

CAS: 30992-29-1

Fórmula: C₉H₁₇NO₄

Peso molecular: 203.24

Ref: 7W-GM2007

α-(Boc-Amino)Isobutyric Acid

CAS: 30992-29-1

α-(Boc-Amino)Isobutyric Acid

Pureza: 98%

Peso molecular: 203.24g/mol

Ref: 54-OR1015473

2-(tert-Butoxycarbonylamino)isobutyric Acid

CAS: 30992-29-1

Fórmula: C₉H₁₇NO₄

Pureza: >98.0%(GC)(T)

Forma y color: White to Almost white powder to crystal

Peso molecular: 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.

Fórmula: C₉H₁₇NO₄

Pureza: Min. 98 Area-%

Forma y color: White Off-White Powder

Peso molecular: 203.24 g/mol

Ref: 3D-FB47799

Boc-2-aminoisobutyric acid

CAS: 30992-29-1

Fórmula: C₉H₁₇NO₄

Pureza: 95%

Forma y color: Solid, White crystalline

Peso molecular: 203.238

Ref: 10-F075038

Boc-α-Methylalanine

Producto controlado

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);

Fórmula: C₉H₁₇NO₄

Forma y color: Neat

Peso molecular: 203.24

Ref: TR-B656940