63649-14-9

Basic information

• Product Name: 5-AMINOPENTANOIC ACID-BENZYL ESTER P-TOSYLATE
• Synonyms: DELTA-AMINOVALERIC ACID-BENZYL ESTER P-TOSYLATE;H-APE(5)-OBZL TOS-OH;H-5-AVA-OBZL TOSOH;5-AMINOVALERIC ACID BENZYL ESTER 4-TOLUENESULFONATE SALT;5-AMINOVALERIC ACID-BENZYL ESTER P-TOSYLATE;5-AMINO-N-PENTANOIC ACID BENZYL ESTER 4-TOLUENESULFONATE SALT;5-AMINOPENTANOIC ACID-BENZYL ESTER P-TOSYLATE;5-Aminopentanoic Acid Benzyl Ester Tosylate
• CAS NO: 63649-14-9
• Molecular Formula: C₇H₈O₃S*C₁₂H₁₇NO₂
• Molecular Weight: 379.47
• Product Categories: All Aliphatics;Aliphatics;Amines;Sulfur & Selenium Compounds
• Mol File: 63649-14-9.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Store at RT.
• Solubility: Dichloromethane, Methanol
• CAS DataBase Reference: 5-AMINOPENTANOIC ACID-BENZYL ESTER P-TOSYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-AMINOPENTANOIC ACID-BENZYL ESTER P-TOSYLATE(63649-14-9)
• EPA Substance Registry System: 5-AMINOPENTANOIC ACID-BENZYL ESTER P-TOSYLATE(63649-14-9)

Safety Data

• Hazardous Substances Data: 63649-14-9(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Upstream product

• 104-15-4 toluene-4-sulfonic acid 
• 100-51-6 benzyl alcohol 
• 660-88-8 5-aminopentanoic acid 

Downstream Products

• 1173377-58-6 Nα-Nε-bis(hexadecanoyl)-N-[4-(benzyloxycarbonyl)butyl]-L-lysinamide 
• 63984-35-0 N-Iodacetyl-δ-aminovaleriansaeure 
• 532926-51-5 benzyl N-BOC-alanyl-5-aminovaleriate 
• 63984-37-2 N-Iodacetyl-δ-aminovaleriansaeurebenzylester 

Relevant articles and documents

DELIVERY OF TARGET SPECIFIC NUCLEASES

Described herein are lipid nanoparticles comprising cationic lipids and other lipids and also comprising engineered nucleases facilitate transfer of nucleic acids to cells.

Molecular structural requirements, dye specificity, and application of anionic peptide amphiphiles that induce intense fluorescence in cationic dyes

We have previously reported that a double-chain anionic amphiphile capable of intermolecular triple hydrogen bonds could form extremely hydrophobic sites in water and specifically incorporated stilbazolium-based compact hemicyanine dyes as monomeric species, resulting in induction of intense fluorescence emission in the dyes. In this paper, the structural requirements of the intense fluorescence-inducing amphiphiles were investigated. It is noted that the introduction of β-Ala residues into two long-chain alkyl group moieties was most effective for the amphiphiles derived from L-glutamic acid with relatively shorter side-chain methylenes. The dye specificity in terms of induction of the intense fluorescence was also investigated using hemicyanines (stilbazolium etc.), cyanine, carbocyanine, thiacarbocyanines, and azo dye. The amphiphile with the shortest octanoyl-β-alanyl double-chain alkyl groups, longer side-chain, and shorter spacer was found to show increased sensitivity to alkali metal ions, especially Li+. This could be a potential OFF-ON type fluorescence sensor for Li+. The Royal Society of Chemistry 2009.

2 AND 3-SUBSTITUTED ENKEPHALINS

Analogs of enkephalin having agonist activity at opiate receptors are disclosed herein. These analogs are useful as analgesics, non-addicting narcotic antagonists and anti-diarrheal agents.