N-Benzyl-D-glucamine

Base Information

• Chemical Name: N-Benzyl-D-glucamine
• CAS No.: 74410-48-3
• Molecular Formula: C13H21 N O5
• Molecular Weight: 271.313
• European Community (EC) Number: 616-092-6
• DSSTox Substance ID: DTXSID801264564
• Nikkaji Number: J263.769C
• Mol file: 74410-48-3.mol

Synonyms:N-Benzyl-D-glucamine;74410-48-3;(2R,3R,4R,5S)-6-(benzylamino)hexane-1,2,3,4,5-pentol;1-Deoxy-1-[(phenylmethyl)amino]-D-glucitol;SCHEMBL7160696;DTXSID801264564

Chemical Property of N-Benzyl-D-glucamine

Chemical Property:

• PSA: 113.18000
• LogP: -1.39700
• XLogP3: -1.9
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 271.14197277
• Heavy Atom Count: 19
• Complexity: 235

Purity/Quality:

98%Min ^*data from raw suppliers

N-BENZYL-D-GLUCAMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CNCC(C(C(C(CO)O)O)O)O
• Isomeric SMILES: C1=CC=C(C=C1)CNC[C@@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O

Technology Process of N-Benzyl-D-glucamine

There total 3 articles about N-Benzyl-D-glucamine 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:

Reference yield: 67.0%

D-mannitol (50-99-7,59-23-4,921-60-8,1949-88-8,1990-29-0,2152-76-3,2595-97-3,2595-98-4,3458-28-4,4205-23-6,5934-56-5,5978-95-0,5987-68-8,6027-89-0,6038-51-3,7635-11-2,10030-80-5,15572-79-9,19163-87-2,23567-25-1,26566-61-0,30077-17-9,31103-86-3,39665-52-6,40866-07-7,58367-01-4,58407-05-9,58407-06-0,83198-69-0,83198-70-3,83198-71-4,93780-23-5,145920-48-5) + benzylamine (100-46-9) → 1-(benzylamino)-1-deoxy-D-mannitol (38709-24-9,74410-48-3,74410-49-4)

Guidance literature:

With hydrogen; platinum(IV) oxide; In methanol; for 24h; Ambient temperature;

DOI:10.1016/S0008-6215(00)85528-7

Reference yield: 64.0%

D-glucose (50-99-7,59-23-4,921-60-8,1949-88-8,1990-29-0,2152-76-3,2595-97-3,2595-98-4,3458-28-4,4205-23-6,5934-56-5,5978-95-0,5987-68-8,6027-89-0,6038-51-3,7635-11-2,10030-80-5,15572-79-9,19163-87-2,23567-25-1,26566-61-0,30077-17-9,31103-86-3,39665-52-6,40866-07-7,58367-01-4,58407-05-9,58407-06-0,83198-69-0,83198-70-3,83198-71-4,93780-23-5,145920-48-5) + benzylamine (100-46-9) → 1-(benzylamino)-1-deoxy-D-galactitol (38709-24-9,74410-48-3,74410-49-4)

Guidance literature:

With hydrogen; platinum(IV) oxide; In methanol; for 24h; Ambient temperature;

DOI:10.1016/S0008-6215(00)85528-7

Reference yield:

D-glucose (50-99-7) + benzylamine (100-46-9) → N-benzyl-1-amino-1-deoxy-D-glucitol (74410-48-3)

Guidance literature:

With water; anschliessendes Hydrieren nach Zusatz von Methanol an Platin;

DOI:10.1021/ja01570a063

upstream raw materials:

D-glucose

benzylamine

D-mannitol

D-glucose

Downstream raw materials:

1-Amino-1-deoxy-D-glucitol

Refernces