102717-16-8

Basic information

• Product Name: 4-Nitrophenyl4,6-cyclohexylidene-b-D-mannopyranoside
• Synonyms: 4-Nitrophenyl4,6-cyclohexylidene-b-D-mannopyranoside;4-Nitrophenyl 4,6-cyclohexylidene-β-D-mannopyranoside;4-Nitrophenyl 4,6-O-cyclohexylidene-beta-D-mannopyranoside
• CAS NO: 102717-16-8
• Molecular Formula: C₁₈H₂₃NO₈
• Molecular Weight: 381.379
• EINECS: 1533716-785-6
• Mol File: 102717-16-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 617.1±55.0 °C(Predicted)
• Appearance: /
• Density: 1.44±0.1 g/cm3(Predicted)
• Solubility: Chloroform, Ethyl Acetate, Methanol
• PKA: 12.53±0.60(Predicted)
• CAS DataBase Reference: 4-Nitrophenyl4,6-cyclohexylidene-b-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Nitrophenyl4,6-cyclohexylidene-b-D-mannopyranoside(102717-16-8)
• EPA Substance Registry System: 4-Nitrophenyl4,6-cyclohexylidene-b-D-mannopyranoside(102717-16-8)

Safety Data

• Hazardous Substances Data: 102717-16-8(Hazardous Substances Data)

Usage

Chemical Properties

Pale Yellow Foam

Uses

p-Nitrophenyl 4,6-Cyclohexylidene-β-D-mannopyranoside (cas# 102717-16-8) is a compound useful in organic synthesis.

Upstream product

• 35599-02-1 4-nitrophenyl-β-D-mannopyranoside 
• 1122-84-5 1-ethoxycyclohexene 

Downstream Products

• 102717-23-7 C₇₉H₆₅NO₁₈ 
• 102717-22-6 C₇₂H₆₁NO₁₇ 
• 102717-24-8 p-nitrophenyl O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1-3)-4-O-benzoyl-2-O-benzyl-β-D-mannopyranoside 
• 102717-20-4 p-nitrophenyl O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1-3)-2-O-benzyl-4,6-O-cyclohexylidene-β-D-mannopyranoside 
• 102717-21-5 p-nitrophenyl O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1-3)-2-O-benzyl-α-D-mannopyranoside 
• 102717-18-0 p-nitrophenyl 3-O-benzoyl-2-O-benzyl-4,6-O-cyclohexylidene-β-D-mannopyranoside 
• 102717-19-1 p-nitrophenyl 2-O-benzyl-4,6-O-cyclohexylidene-β-D-mannopyranoside 
• 102717-17-9 p-nitrophenyl 3-O-benzoyl-4,6-O-cyclohexylidene-β-D-mannopyranoside 

Relevant articles and documents

p-Trifluoroacetamidophenyl O-alpha-D-mannopyranosyl-(1----3)-O-[alpha-D-mannopyranosyl- (1----6)]-beta-D-mannopyranoside.

p-Nitrophenyl 2-O-benzyl-4,5-O-cyclohexylidene-beta-D-mannopyranoside (4) was condensed with tetra-O-benzoyl-alpha-D-mannopyranosyl bromide. The resulting, protected disaccharide was converted into p-nitrophenyl O-(2,3,4-tri-O-benzoyl-alpha-D-mannopyranos