38257-96-4

Basic information

• Product Name: 1-Octanol, 8-(triphenylmethoxy)-
• CAS NO: 38257-96-4
• Molecular Formula: C27H32O2
• Molecular Weight: 388.55
• Mol File: 38257-96-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-Octanol, 8-(triphenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octanol, 8-(triphenylmethoxy)-(38257-96-4)
• EPA Substance Registry System: 1-Octanol, 8-(triphenylmethoxy)-(38257-96-4)

Safety Data

• Hazardous Substances Data: 38257-96-4(Hazardous Substances Data)

Upstream product

• 629-41-4 1,8-Octanediol 
• 76-83-5 trityl chloride 
• 153164-83-1 8-allyloxyoctan-1-ol 
• 1403675-03-5 1-allyloxy-8-trityloxyoctane 
• 153164-82-0 1-(allyloxy)-8-(prop-2-yn-1-yloxy)octane 

Downstream Products

• 65686-45-5 Methanesulfonic acid 8-trityloxy-octyl ester 
• 745073-50-1 1-(benzyloxy)methyl-3,14-dioxabicyclo[10.2.1]pentadec-11(E)-ene-4,13-dione 
• 745073-43-2 5-(benzyloxy)methyl-3-[(E)-8-carboxyheptylidene]-5-hydroxymethyltetrahydro-2-furanone 
• 745073-29-4 5-(benzyloxy)methyl-3-[(E)-8-hydroxyoctylidene]-5-(4-methoxyphenoxy)methyltetrahydro-2-furanone 
• 745073-36-3 5-(benzyloxy)methyl-3-[(E)-8-carboxyheptylidene]-5-(4-methoxyphenoxy)methyltetrahydro-2-furanone 
• 745073-22-7 5-(benzyloxy)methyl-5-(4-methoxyphenoxy)methyl-3-[(E)-8-trityloxyoctylidene]tetrahydro-2-furanone 
• 213768-46-8 Methanesulfonic acid 8-[(2R,3R,4S,5S,6S)-4-allyloxy-3-benzyloxy-6-methoxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-trityloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-ylmethoxy]-octyl ester 
• 213767-62-5 methyl 3-O-allyl-2-O-[2',3',4'-tri-O-benzyl-6'-O-(8''-trityloxyoctyl)-α-D-galactopyranosyl]-4-O-benzyl-6-O-methanesulfonyl-α-D-mannopyranoside 
• 213768-39-9 (1S,3R,4R,5S,6S,7R,20R,22S,23S,24R)-4,5,6,24-Tetrakis-benzyloxy-23-((2R,3R,5R,6R)-3,5-bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-22-methoxy-2,9,18,21,25-pentaoxa-tricyclo[18.2.2.1^3,7]pentacosane 
• 213767-80-7 methyl 3-O-allyl-2-O-[2',3',4'-tri-O-benzyl-6'-O-(8''-hydroxyoctyl)-α-D-galactopyranosyl]-4-O-benzyl-6-O-methanesulfonyl-α-D-mannopyranoside 
• 213768-53-7 Methanesulfonic acid 8-[(2R,3R,4S,5S,6S)-4-allyloxy-3-benzyloxy-6-methoxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-ylmethoxy]-octyl ester 
• 213768-01-5 methyl 2-O-(3'-O-allyl-4'-O-benzyl-α-D-galactopyranosyl)-2,3,4-tri-O-benzyl-6,6'-di-O-(octane-1,8-diyl)-α-D-mannopyranoside 
• 213768-21-9 methyl 2-O-(2',3',4'-tri-O-benzyl-α-D-galactopyranosyl)-4-O-benzyl-6,6'-di-O-(octane-1,8-diyl)-α-D-mannopyranoside 
• 213766-30-4 ethyl 2,3,4-tri-O-benzyl-6-O-(8'-trityloxyoctyl)-1-thio-α-D-galactopyranoside 

Relevant articles and documents

A new class of organogelators based on triphenylmethyl derivatives of primary alcohols: Hydrophobic interactions alone can mediate gelation

In the present work, we have explored the use of the triphenylmethyl group, a commonly used protecting group for primary alcohols as a gelling structural component in the design of molecular gelators. We synthesized a small library of triphenylmethyl deri

Elaboration of the ether cleaving ability and selectivity of the classical Pearlman's catalyst [Pd(OH)2/C]: Concise synthesis of a precursor for a myo-inositol pyrophosphate

The cleavage of propargyl, allyl, benzyl, and PMB ethers by Pd(OH) 2/C can be tuned in that order, by varying the reaction conditions. Other moieties such as C-C double bonds, esters, trityl ether, p-bromo and p-nitrobenzyl ethers are stable to these reaction conditions. Cleavage of allyl ethers can be made catalytic by using 1:1 mixture of Pd(OH)2/C and Pd/C. The synthetic potential of the selective ether cleaving ability of Pd(OH)2/C, essentially under neutral conditions, has been demonstrated by an efficient synthesis of a precursor for the preparation of an inositol pyrophosphate derivative.

N1-substituted thymine derivatives as mitochondrial thymidine kinase (TK-2) inhibitors

Novel N1-substituted thymine derivatives related to 1-[(Z)-4-(triphenylmethoxy)-2-butenyl]thymine have been synthesized and evaluated against thymidine kinase-2 (TK-2) and related nucleoside kinases [i.e., Drosophila melanogaster deoxynucleosid