106820-14-8

Basic information

• Product Name: 2,3,4-TRI-O-ACETYL-D-RIBONONITRILE
• Synonyms: 2,3,4-TRI-O-ACETYL-D-RIBONONITRILE
• CAS NO: 106820-14-8
• Molecular Formula: C₁₁H₁₆O₈
• Molecular Weight: 273.2393
• Mol File: 106820-14-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3,4-TRI-O-ACETYL-D-RIBONONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4-TRI-O-ACETYL-D-RIBONONITRILE(106820-14-8)
• EPA Substance Registry System: 2,3,4-TRI-O-ACETYL-D-RIBONONITRILE(106820-14-8)

Safety Data

• Hazardous Substances Data: 106820-14-8(Hazardous Substances Data)

Usage

Type of compound

Nitrile derivative

Common use

Organic synthesis and chemical research

Structural feature

Acetyl groups attached to the ribononitrile molecule

Chemical properties

Distinct due to the presence of acetyl groups

Role

Precursor in the synthesis of various organic compounds and pharmaceutical drugs

Application

Reagent in the production of synthetic peptides and other biochemical applications
Please note that the material provided does not include specific values for properties such as melting point, boiling point, solubility, or reactivity. These properties can vary depending on the specific conditions and context in which the compound is used.

Upstream product

• 87-72-9 D-Xylose 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Downstream Products

• 1233-03-0 1,2,3,4-tetra-O-acetyl-L-arabinopyranose 
• 869848-87-3 2,3,4-tri-O-acetyl-β-L-arabinopyranosyl trichloroacetimidate 
• 475101-58-7 4-methoxyphenyl 2,3-O-isopropylidene β-D-xylopyranoside 
• 13299-09-7 p-Methoxyphenyl β-D-xylopyranoside 
• 13299-05-3 p-Methoxyphenyl 2,3,4-tri-O-acetyl-β-D-xylopyranoside 
• 52544-91-9 (2S,3R,4S,5R)-2-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 869848-87-3 C₁₃H₁₆Cl₃NO₈ 
• 66912-32-1 4-Methylumbelliferyl-β-D-ribopyranosid 
• 6734-33-4 4-methylumbellifer-7-yl β-D-xylopyranoside 
• 128376-91-0 2,3,4-tri-O-acetyl-α-D-xylopyranosyl trichloroacetimidate 
• 132247-84-8 (1S,2S,3R)-5-oxo-N-phenyl-3-(2',3',4'-tri-O-acetyl-α-D-xylopyranosyloxy)cyclohexane-1,2-dicarboximide 
• 132247-84-8 (1R,2R,3S)-5-oxo-N-phenyl-3-(2',3',4'-tri-O-acetyl-β-D-xylopyranosyloxy)cyclohexane-1,2-dicarboximide 

Relevant articles and documents

SYNTHESE EN SERIE D-XYLOPYRANOSE: TRI-O-ACETYL-D-XYLOSES ET DERIVES CHLOROACETYLES

Selective acetylation of D-xylose with acetic anhydride in dry pyridine at -30 deg C gave 1,2,3- and 1,2,4-tri-O-acetyl-α-D-xylopyranose with traces of 2,3,4-tri-O-acetyl-D-xylopyranose.Acetylation of D-xylose under conditions differing from the preceding ones only with respect to an azotropic distillation of an excess of pyridine before addition of acetic anhydride afforded a mixture of the eight possible triacetates.Unambiguous synthesis of 1,2,3-, 1,2,4-, and 1,3,4-tri-O-acetyl-β-D-xylopyranose was obtained from 3,4-di-O-acetyl-1,2-O-(1-ethoxyethylidene)-α-D-xylopyranose, which also gave 1,3,4-tri-O-acetyl-α-D-xylopyranose.The aforementioned O-acetyl derivatives and the derived monochloroacetyl compounds were analyzed by 13C- and 1H-n.m.r. spectroscopy at 62.86 and 250 MHz, respectively.