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D-Mannose phenylhydrazone

Base Information
  • Chemical Name:D-Mannose phenylhydrazone
  • CAS No.:6147-14-4
  • Molecular Formula:C12H18N2O5
  • Molecular Weight:270.285
  • Hs Code.:
  • NSC Number:243591,19778
  • Mol file:6147-14-4.mol
D-Mannose phenylhydrazone

Synonyms:D-Mannose phenylhydrazone;D-Mannosephenylhydrazine;6147-14-4;D-Mannose, phenylhydrazone;Mannose, phenylhydrazone, D-;NSC 19778;(6E)-6-(phenylhydrazinylidene)hexane-1,2,3,4,5-pentol;962-53-8;NSC19778;NSC-19778;NSC243591;NSC-243591

Suppliers and Price of D-Mannose phenylhydrazone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 3 raw suppliers
Chemical Property of D-Mannose phenylhydrazone
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:195.5°C 
  • Refractive Index:1.4760 (estimate) 
  • Boiling Point:620.471°C at 760 mmHg 
  • Flash Point:329.049°C 
  • PSA:125.54000 
  • Density:1.399g/cm3 
  • LogP:-1.40680 
  • Water Solubility.:10.3g/L(100 oC) 
  • XLogP3:-0.7
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:7
  • Exact Mass:270.12157168
  • Heavy Atom Count:19
  • Complexity:271
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)NN=CC(C(C(C(CO)O)O)O)O
  • Isomeric SMILES:C1=CC=C(C=C1)N/N=C/C(C(C(C(CO)O)O)O)O
Technology Process of D-Mannose phenylhydrazone

There total 1 articles about D-Mannose phenylhydrazone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
upstream raw materials:

galactose

phenylhydrazine

Downstream raw materials:

galactose

Refernces

Some Amines Derived from 3-Phenyl-1-indanone

10.1021/ja01646a074

The study explores the isomerization of D-glucose to D-mannose using a resin catalyst in carbon dioxide-free water under nitrogen, yielding D-mannose phenylhydrazone. It also investigates the synthesis of amines derived from 3-phenyl-1-indanone through the Mannich reaction with various amines (dimethylamine, diethylamine, piperidine, and morpholine) and formaldehyde, resulting in low yields and unstable products. Further reductions and hydrogenations of these products led to the formation of indene derivatives and aminoalcohols, but no significant pharmacologic activity was observed. Additionally, the study examines the Mannich reaction of p-nitroacetophenone with different amines and formaldehyde, yielding p-(di)-alkylamino-p-nitropropiophenones, which were further reduced to aminoketones and reacted with phenylhydrazine to form pyrazolines.

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