24070-16-4

Basic information

• Product Name: 2-(Trityl-Amino)-Ethanol
• Synonyms: 2-(Trityl-Amino)-Ethanol;N-Tritylethanolamine;Ethanol, 2-[(triphenylmethyl)amino]-;2-(Trityl-Amino)-Ethanol(WX640271)
• CAS NO: 24070-16-4
• Molecular Formula: C₂₁H₂₁NO
• Molecular Weight: 303.39754
• Mol File: 24070-16-4.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(Trityl-Amino)-Ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(Trityl-Amino)-Ethanol(24070-16-4)
• EPA Substance Registry System: 2-(Trityl-Amino)-Ethanol(24070-16-4)

Safety Data

• Hazardous Substances Data: 24070-16-4(Hazardous Substances Data)

Usage

General Description

2-(Trityl-Amino)-Ethanol is a chemical compound with the molecular formula C26H25NO. It is a derivative of ethanol and contains a trityl-protected amino group. 2-(Trityl-Amino)-Ethanol is commonly used in organic synthesis as a protecting group for amines, allowing for selective reactions in the presence of other functional groups. It is also used as a reagent in the preparation of various pharmaceutical and bioactive compounds. Additionally, 2-(Trityl-Amino)-Ethanol has applications in the field of peptide and protein chemistry, where it can be used for the synthesis and modification of peptides and proteins.

Upstream product

• 76-83-5 trityl chloride 
• 141-43-5 ethanolamine 
• 75-21-8 oxirane 
• 5824-40-8 Triphenylmethylamin 
• 2002-24-6 2-amino-ethanol hydrochloride 
• 121-44-8 triethylamine 
• 75-05-8 acetonitrile 
• 596-43-0 bromo-triphenyl-methane 

Downstream Products

• 64350-19-2 N-Trityl O-(1,2-disteaoryl-sn-glycero-3-phosphoryl)-ethanolamin 
• 69747-56-4 (Z)-Octadec-9-enoic acid 2-{hydroxy-[2-(trityl-amino)-ethoxy]-phosphoryloxy}-1-((Z)-octadec-9-enoyloxymethyl)-ethyl ester 
• 156366-26-6 ethyl 4-(2'-(N-tritylamino)ethoxy)acetoacetate 
• 1431463-05-6 2-(2-(tritylamino)ethyl)isoindoline-1,3-dione 
• 1204669-82-8 4-(3-chloro-4-fluorophenyl)-3-(4-{[2-(tritylamino)ethyl]amino}-1,2,5-oxadiazol-3-yl)-1,2,4-oxadiazol-5(4H)-one 
• 1438408-97-9 C₃₃H₃₀N₂O₂S₂ 
• 1446424-94-7 C₃₁H₂₆N₂O₃S 
• 1446424-93-6 C₃₁H₂₆N₂O₃S 
• 1438408-80-0 C₃₃H₃₀N₂O₃S 
• 1438409-74-5 3-(2-(tritylamino)ethyl)thiazolidine-2,4-dione 
• 102152-59-0 Hexadecanoic acid (R)-1-hexadecanoyloxymethyl-2-{methoxy-[2-(trityl-amino)-ethoxy]-thiophosphoryloxy}-ethyl ester 
• 102152-58-9 Hexadecanoic acid (R)-1-hexadecanoyloxymethyl-2-{methoxy-[2-(trityl-amino)-ethoxy]-phosphoryloxy}-ethyl ester 

Relevant articles and documents

1,2,4-Thiadiazole acyclic nucleoside phosphonates as inhibitors of cysteine dependent enzymes cathepsin K and GSK-3β

In analogy to antiviral acyclic nucleoside phosphonates, a series of 5-amino-3-oxo-1,2,4-thiadiazol-3(2H)-ones bearing a 2-phosphonomethoxyethyl (PME) or 3-hydroxy-2-(phosphonomethoxy)propyl (HPMP) group at the position 2 of the heterocyclic moiety has be

Pyrrole-Based Anion-Responsive π-Electronic Molecules as Hydrogen-Bonding Catalysts

The abilities of dipyrrolyldiketone boron complexes as hydrogen-bonding donor organocatalysts were examined by the Mannich-type reaction of N-acyl heteroarenium chlorides with 1-methoxy-2-methyl-1-trimethylsiloxy-1-propene, as well as by the classical N-alkylation of amines with trityl chloride under base-free conditions. 1H NMR examinations of the hydrogen-bonding interaction between the pyrrole NH of the catalyst and the Cl- in the N-acyl heteroarenium salt suggested that the activation of N-acyl heteroarenium chlorides occurs through anion binding by the catalyst.

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