6292-90-6

Basic information

• Product Name: L-TYROSINE BUTYL ESTER
• Synonyms: L-TYROSINE BUTYL ESTER;3-(4-Hydroxyphenyl)-L-alaninebutylester
• CAS NO: 6292-90-6
• Molecular Formula: C₁₃H₁₉NO₃
• Molecular Weight: 237.29
• Mol File: 6292-90-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 370.2 °C at 760 mmHg
• Flash Point: 177.7 °C
• Appearance: /
• Density: 1.125 g/cm³
• Vapor Pressure: 5.28E-06mmHg at 25°C
• Refractive Index: 1.539
• CAS DataBase Reference: L-TYROSINE BUTYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: L-TYROSINE BUTYL ESTER(6292-90-6)
• EPA Substance Registry System: L-TYROSINE BUTYL ESTER(6292-90-6)

Safety Data

• Hazardous Substances Data: 6292-90-6(Hazardous Substances Data)

Usage

General Description

L-Tyrosine Butyl Ester is a chemical compound derived from Tyrosine, an amino acid that plays a key role in protein synthesis in the body. It is considered to be an ester, which is a compound produced by the reaction between an acid and an alcohol, often resulting in a sweet or fruity smell. This particular ester is produced using Tyrosine and Butanol. It is primarily utilized in the field of biochemistry, often in research and laboratory settings. Potential health effects or uses of L-Tyrosine Butyl Ester remain largely unexplored and as such, it should be handled with caution until more definitive information about its properties and safety is available.

InChI:InChI=1/C13H19NO3/c1-2-3-8-17-13(16)12(14)9-10-4-6-11(15)7-5-10/h4-7,12,15H,2-3,8-9,14H2,1H3

Upstream product

• 60-18-4 L-tyrosine 
• 71-36-3 butan-1-ol 

Downstream Products

• 169319-70-4 (S)-2-{[1-((S)-2-Acetylsulfanyl-3-methyl-butyrylamino)-cyclopentanecarbonyl]-amino}-3-(4-hydroxy-phenyl)-propionic acid butyl ester 
• 169319-98-6 (S)-3-(4-Hydroxy-phenyl)-2-{[1-((S)-2-mercapto-3-methyl-butyrylamino)-cyclopentanecarbonyl]-amino}-propionic acid butyl ester 
• 1027260-72-5 (S)-2-[(1-tert-Butoxycarbonylamino-cyclopentanecarbonyl)-amino]-3-(4-hydroxy-phenyl)-propionic acid butyl ester 

Relevant articles and documents

First Total Synthesis of the Marine-Derived Anti-inflammatory Natural Product (-)-Herdmanine D through a Steglich Esterification

An efficient and regioselective route for the first total synthesis of the antiinflammatory marine natural product ( )-herdmanine D, with an excellent overall yield of 18%, is described. A key feature of the synthetic strategy is a Steglich esterification of regioselectively constructed 6-bromo-5-methoxy-1H-indole-3-carboxylic acid with protected L-tyrosine. The formation of the L-isomer was confirmed through measurement of the optical activity. The current strategy paves the way for the construction of diverse analogues of ( )-herdmanine D for drug development.