(3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL

Base Information

• Chemical Name: (3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL
• CAS No.: 280745-41-7
• Molecular Formula: C₆H₁₃NO₄
• Molecular Weight: 163.174
• Mol file: 280745-41-7.mol

Synonyms:(3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL;(3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL SALT;(3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HYDROCHLORIDE;1H-Azepine-3,4,5,6-tetrol, hexahydro-, (3S,4S,5S,6S)-

Chemical Property of (3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL

Chemical Property:

• Boiling Point: 328.6±42.0 °C(Predicted)
• PKA: 13.54±0.70(Predicted)
• PSA: 92.95000
• Density: 1.508±0.06 g/cm3(Predicted)
• LogP: -1.83600

Purity/Quality:

98% ^*data from raw suppliers

(3S,4S,5S,6S)-3,4,5,6-Tetrahydroxyazepane hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of (3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL

There total 83 articles about (3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL 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: 100.0%

N-benzyl-3,4-di-O-benzyl-1,6-dideoxy-1,6-imino-L-iditol (157363-87-6) → 1,6-dideoxy-1,6-imino-(2S,3R,4R,5S)-L-iditol (16647-61-3,280745-41-7)

Guidance literature:

With hydrogen; palladium; In acetic acid; for 15h;

DOI:10.1016/S0040-4039(00)76888-2

Reference yield: 92.0%

(3S,4R,5R,6S)-N-diphenylmethyl-3,4,5,6-tetrahydroxyazepane (676259-81-7,280745-40-6) → 1,6-dideoxy-1,6-imino-(2S,3R,4R,5S)-L-iditol (16647-61-3,280745-41-7)

Guidance literature:

With hydrogen; palladium dihydroxide; In methanol; for 14h;

DOI:10.1016/j.bmc.2003.10.003

Reference yield: 80.0%

(3S,4R,5R,6S)-N-allyl-4,5-di-O-allyl-3,4,5,6-tetrahydroxyazepane (178909-10-9) → 1,6-dideoxy-1,6-imino-(2S,3R,4R,5S)-L-iditol (16647-61-3,280745-41-7)

Guidance literature:

With perchloric acid; palladium on activated charcoal; In methanol; for 8h; Heating;

DOI:10.1016/S0968-0896(96)00218-0

upstream raw materials:

6-Azido-6-desoxy-D-glucopyranose

(3R,4R,5R,6S)-3,4,5,6-tetrahydroxy-4,5-O-isopropylidene azepane

6-deoxy-6-N-benzyloxycarbonyl-1,2-O-isopropylidene-3-O-phenylmethyl-α-D-gluco-1,4-furanose

3-O-benzyl-6-deoxy-1,2-O-isopropylidene-6-nitro-α-D-gluco-furanose

Downstream raw materials:

(3R,4R,5R,6R)-3,4,5,6-Tetraacetoxy-N-acetylazepane

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