101642-77-7

Basic information

• Product Name: Cbz-DL-3-Aminoisobutyric acid
• Synonyms: Cbz-DL-3-Aminoisobutyric acid;3-(benzyloxycarbonylamino)-2-methylpropanoic acid;REF DUPL: Cbz-DL-3-Aminoisobutyric acid
• CAS NO: 101642-77-7
• Molecular Formula: C₁₂H₁₅NO₄
• Molecular Weight: 237.2518
• Mol File: 101642-77-7.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Cbz-DL-3-Aminoisobutyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: Cbz-DL-3-Aminoisobutyric acid(101642-77-7)
• EPA Substance Registry System: Cbz-DL-3-Aminoisobutyric acid(101642-77-7)

Safety Data

• Hazardous Substances Data: 101642-77-7(Hazardous Substances Data)

Usage

General Description

Cbz-DL-3-Aminoisobutyric acid, also known as N-[(benzyloxy)carbonyl]-DL-α-aminoisobutyric acid, is an organic compound that acts as an important reagent in the field of organic chemistry and biochemistry. This non-proteinogenic amino acid has a role in the synthesis of peptides and it's often used as a building block in the peptide synthesis process. The abbreviation "Cbz" stands for "carboxybenzyl," indicating it's a protected derivative, a factor that helps stabilize the compound before it can react with other substances. Its molecular formula is C12H15NO4 and it has a molar mass of 237.25 g/mol.

Upstream product

• 10569-72-9 DL-3-aminoisobutyric acid 
• 501-53-1 benzyl chloroformate 
• 117903-81-8 2-(2'-cyanoprop-2'-enyl)-1H-isoindole-1,3(2H)-dione 
• 28267-25-6 (RS)-2-(aminomethyl)propanoic acid hydrochloride 
• 92932-15-5 2-(2'-cyanopropyl)-1H-isoindole-1,3(2H)-dione 
• 67799-90-0 diethyl 2-(N-methylphthalimido)-2-methylmalonate 

Relevant articles and documents

Synthesis and conformational analysis of 1,3,2-diazaphosphorino[6,1-a] isoquinolines, a new ring system

Through ring-closure reactions of N- or 1′-substituted 1-(2′-aminoethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolines (5a-e) with phenylphosphonyl dichloride, 1- or 3-substituted 4-phenyl-1,3,4,6,7,11b- tetrahydro-2H-1,3,2-diazaphosphorino[6,1-a]isoquinolin-4-one diastereomers (7a-e and 8a-c,e), the first representatives of a new ring system, were prepared. The diastereomeric ratios in the cyclizations and the conformer (A-E) populations of the nitrogen-bridged tricyclic systems (7 and 8) were strongly influenced by the N- and 1′-substituents of the starting diamines. The conformational analysis of compounds 7 and 8 was performed by 1H, 13C and 31P NMR methods.

DELTA-AMINO-GAMMA-HYDROXY-OMEGA-ARYL-ALKANOIC ACID AMIDES

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Chartreusin derivatives and salts thereof

This invention relates to a novel chartreusin derivative of the general formula (I): STR1 and a salt thereof. This chartreusin derivative and a salt thereof have an excellent antitumor activity, which is exhibited even when the site of cancer inoculation