40829-04-7

Basic information

• Product Name: D-Tyrosinol hydrochloride
• Synonyms: L-TYROSINOL HCL;D-TYROSINOL HCL;D-TYROSINOL HYDROCHLORIDE;H-D-TYR-OL HCL;H-TYR-OL HCL;H-L-TYR-OL HCL;(R)-3-(4-HYDROXYPHENYL)-2-AMINO-1-PROPANOL HCL;(R)-BETA-AMINO-4-HYDROXYBENZENEPROPANOL HYDROCHLORIDE
• CAS NO: 40829-04-7
• Molecular Formula: C9H14ClNO2
• Molecular Weight: 203.67
• Product Categories: Amino Acid Derivatives;Amino Alcohols;Peptide Synthesis
• Mol File: 40829-04-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 167 °C
• Boiling Point: 398.8 °C at 760 mmHg
• Flash Point: 195 °C
• Appearance: white to off-white granular powder
• Storage Temp.: 0-6°C
• CAS DataBase Reference: D-Tyrosinol hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: D-Tyrosinol hydrochloride(40829-04-7)
• EPA Substance Registry System: D-Tyrosinol hydrochloride(40829-04-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36-37/39
• WGK Germany: 3
• Hazardous Substances Data: 40829-04-7(Hazardous Substances Data)

Usage

Uses

D-Tyrosinol hydrochloride is a useful reagent and reactant for organic reactions and synthesis.

InChI:InChI=1/C9H13NO2.ClH/c10-8(6-11)5-7-1-3-9(12)4-2-7;/h1-4,8,11-12H,5-6,10H2;1H/t8-;/m1./s1

Upstream product

• 60-18-4 L-tyrosine 
• 102440-13-1 (+/-)-2-amino-3-(4-hydroxy-phenyl)-propan-1-ol; hydrochloride 
• 3417-91-2 L-tyrosine methyl ester HCl 

Downstream Products

• 616884-63-0 OMDM-1 
• 616884-63-0 OMDM-2 
• 1513888-66-8 (S)-8-((1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)amino)-8-oxooctanoic acid 
• 1513888-54-4 (S)-N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)propionamide 
• 1513888-58-8 (S)-N-(1-methoxy-3-(4-methoxyphenyl)propan-2-yl)propionamide 
• 1513888-55-5 (S)-4-(3-hydroxy-2-propionamidopropyl)phenyl propionate 
• 1513888-57-7 (S)-3-(4-hydroxyphenyl)-2-propionamidopropyl propionate 
• 126257-06-5 (S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)propionamide 
• 1513888-60-2 (S)-4-(3-hydroxy-2-(propylamino)propyl)phenol 
• 126455-12-7 (S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)benzamide 
• 1513888-78-2 (S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)hex-5-ynamide 
• 1513888-63-5 (S)-4-(1-(adamantan-1-yl)-1H-1,2,3-triazol-4-yl)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)butanamide 
• 1513888-70-4 4-((2S)-3-hydroxy-2-((9Z,12Z)-octadeca-9,12-dien-1-ylamino)propyl)phenol 
• 1513888-71-5 4-((2S)-3-hydroxy-2-((9Z,12Z,15Z)-octadeca-9,12,15-trien-1-ylamino)propyl)phenol 

Relevant articles and documents

Heterogeneous Catalytic Hydrogenation of Chiral Amino Acid Methyl Esters to Amino Alcohols with Retention of Configuration Over Mg-Modified Cu/ZnO/Al2O3 Catalyst

Selective hydrogenation of amino acid methyl esters to chiral amino alcohols is an important and fascinating process. The CuZn0.3Mg0.1AlOx catalyst for the synthesis of chiral amino alcohols was prepared by the fractional

Synthesis of lipoamino acids and their activity against cerebral ischemic injury

A series of lipoamino acids were synthesized and their neuroprotective effect against brain ischemia induced by oxygen-glucose deprivation (OGD) on rat cerebral slices was evaluated. Among these compounds, N-stearoyl-L-tyrosine (4), N-stearoyl-L-serine (5) and N-stearoyl-L-threonine (6) exhibited good neuroprotective activity. We found that the neuroprotective activity of lipoamino acids depended on the acyl group, the presence of a free carboxylic function and a free hydroxyl group at the branched chain of the amino acids. The results also showed that 5 was the most active compound, protecting rat brain slices against OGD as well as hydrogen peroxide (H2O2) insult at the range of 1-10 M.