126229-90-1

Basic information

• Product Name: Benzoic acid, 3,4,5-tris(octadecyloxy)-
• CAS NO: 126229-90-1
• Molecular Formula: C61H114O5
• Molecular Weight: 927.573
• Mol File: 126229-90-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3,4,5-tris(octadecyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,4,5-tris(octadecyloxy)-(126229-90-1)
• EPA Substance Registry System: Benzoic acid, 3,4,5-tris(octadecyloxy)-(126229-90-1)

Safety Data

• Hazardous Substances Data: 126229-90-1(Hazardous Substances Data)

Upstream product

• 831-61-8 Ethyl gallate 
• 149-91-7 3,4,5-trihydroxybenzoic acid 
• 1268837-82-6 C₆₃H₁₁₈O₅ 
• 112-89-0 1-Bromooctadecane 
• 99-24-1 methyl galloate 
• 188685-33-8 methyl [3,4,5-tris(n-octadecan-1-yloxy)]benzoate 
• 121-79-9 Propyl gallate 

Downstream Products

• 1268837-86-0 C₆₇H₁₁₇NO₇ 
• 1268837-88-2 C₆₇H₁₁₉NO₅ 
• 1447447-01-9 N-ethyl-3,4,5-tris(octadecyloxy)benzamide 
• 1447447-03-1 N-(3-(ethylamino)-3-oxopropyl)-3,4,5-tris(octadecyloxy)benzamide 
• 1447447-02-0 N-(5-acetamidopentyl)-3,4,5-tris(octadecyloxy)benzamide 
• 1447447-00-8 N-(2-acetamidoethyl)-3,4,5-tris(octadecyloxy)benzamide 
• 1447446-97-0 N-(2-aminoethyl)-3,4,5-tris(octadecyloxy)benzamide hydrochloride 

Relevant articles and documents

SYNTHESIS OF OLIGONUCLEOTIDES AND RELATED COMPOUNDS

Methods of synthesizing oligonucleotides via new intermediates on a cleavable support having an azidomethyl moiety are disclosed. The method comprises multiple reaction cycles, each of which comprises sequential coupling a nucleoside or oligonucleotide su

METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID

In this method, an oligonucleotide is prepared by using, as a synthesis unit, a novel nucleoside monomer compound represented by formula (I) [wherein X, R1, Y, Base, Z, Ar, R2, R3 and n are each as defined in Claim 1]. The

Liquid-phase RNA synthesis by using alkyl-chain-soluble support

Recent progress in the RNA therapeutics has increased demand for the synthesis of large quantities of oligoribonucleotides. The assembly of RNA oligomers relies mainly on solid-phase approaches. These allow rapid product purification and the ability to drive a target reaction to completion through the use of excess reagents. Despite the known advantages of solid-phase synthesis, some issues in the process remain to be addressed, such as low and limited scale, reagent accessibility, and the use of a very large excess of reagents. Herein, we report a highly efficient and practical method of liquid-phase synthesis of RNA oligomers by using alkyl-chain-soluble support. We demonstrate the utility of the liquid-phase method through 21-mer RNA synthesis on a gram scale. The assembly of RNA oligomers relies principally on solid-phase approaches, although some alternative methods have been developed to date. A highly efficient and practical method of liquid-phase synthesis for RNA oligomers by using an alkyl-chain-type soluble support is reported. The utility of the liquid-phase method through 21-mer RNA synthesis on a gram scale is described (see scheme). Copyright