CAS 30992-29-1

N-[(1,1-Dimethylethoxy)carbonyl]-2-methylalanine

Description:

N-[(1,1-Dimethylethoxy)carbonyl]-2-methylalanine, with the CAS number 30992-29-1, is an amino acid derivative characterized by the presence of a carbonyl group and a bulky dimethylethoxy protecting group. This compound typically exhibits properties associated with amino acids, such as the ability to form hydrogen bonds and participate in various chemical reactions due to its functional groups. The dimethylethoxy group enhances its lipophilicity, which can influence its solubility in organic solvents compared to water. Additionally, the presence of the methyl group on the alpha carbon contributes to its steric properties, potentially affecting its reactivity and interactions in biological systems. This compound is often utilized in peptide synthesis and other organic synthesis applications, where the protection of functional groups is crucial for selective reactions. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, making it important to consider these conditions during handling and experimentation.

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

Synonyms:

• 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

Purity: 98+%

Color and Shape: White, Crystals or powder or crystalline powder

Molecular weight: 202.23

Ref: 02-L19484

Boc-Aib-OH

CAS: 30992-29-1

Bachem ID: 4010082.

Formula: C₉H₁₇NO₄

Purity: > 99%

Color and Shape: White

Molecular weight: 203.24

Ref: 01-4010082

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

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 203.2356

Ref: IN-DA003OFR

Boc-Aib-OH

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Molecular weight: 203.24

Ref: 7W-GM2007

α-(Boc-Amino)Isobutyric Acid

CAS: 30992-29-1

α-(Boc-Amino)Isobutyric Acid

Purity: 98%

Molecular weight: 203.24g/mol

Ref: 54-OR1015473

2-(tert-Butoxycarbonylamino)isobutyric Acid

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Purity: >98.0%(GC)(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 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

Purity: Min. 98 Area-%

Color and Shape: White Off-White Powder

Molecular weight: 203.24 g/mol

Ref: 3D-FB47799

Boc-2-aminoisobutyric acid

CAS: 30992-29-1

Formula: C₉H₁₇NO₄

Purity: 95%

Color and Shape: Solid, White crystalline

Molecular weight: 203.238

Ref: 10-F075038

Boc-α-Methylalanine

Controlled Product

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

Color and Shape: Neat

Molecular weight: 203.24

Ref: TR-B656940