(2S,3S,4R)-2,3,4,5-tetrahydroxypentanal

Base Information

• Chemical Name: (2S,3S,4R)-2,3,4,5-tetrahydroxypentanal
• CAS No.: 532-20-7
• Deprecated CAS: 80952-57-4
• Molecular Formula: C₅H₁₀O₅
• Molecular Weight: 150.131
• European Community (EC) Number: 214-212-8
• UNII: M795K6HJOL
• DSSTox Substance ID: DTXSID601018943
• Nikkaji Number: J82.119E
• Wikidata: Q56219426
• Metabolomics Workbench ID: 50647
• Mol file: 532-20-7.mol

Synonyms:lyxose;lyxose, (D)-isomer;lyxose, (L)-isomer

Chemical Property of (2S,3S,4R)-2,3,4,5-tetrahydroxypentanal

Chemical Property:

• Boiling Point: 375.4±42.0 °C(Predicted)
• PKA: 12.16±0.70(Predicted)
• PSA: 0.00000
• Density: 1.681±0.06 g/cm3(Predicted)
• LogP: 0.00000
• XLogP3: -2.3
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 150.05282342
• Heavy Atom Count: 10
• Complexity: 104

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Chemical Classes: Biological Agents -> Monosaccharides and Derivatives
• Canonical SMILES: C(C(C(C(C=O)O)O)O)O
• Isomeric SMILES: C([C@H]([C@@H]([C@@H](C=O)O)O)O)O

Technology Process of (2S,3S,4R)-2,3,4,5-tetrahydroxypentanal

There total 174 articles about (2S,3S,4R)-2,3,4,5-tetrahydroxypentanal 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:

3-O-α-L-rhamnopyranosyl polygalacic acid {28-O-α-L-rhamnopyranosyl(1→3)-β-D-xylopyranosyl(1→4)-α-L-rhamnopyranosyl(1→2)-[α-L-arabinofuranosyl(1→ 2)]-β-D-fucopyranosyl} ester → D-Xylose (87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2) + L-rhamnose (73-34-7) + L-arabinose (532-20-7,613-83-2,7261-25-8,7687-39-0,13221-22-2,14795-83-6,15761-67-8,20074-49-1,25545-03-3,25545-04-4,32445-75-3,34436-17-4,36441-93-7,36468-53-8,37110-85-3,37388-49-1,38029-69-5,40461-77-6,40461-89-0,41546-19-4,41546-20-7,41546-21-8,41546-26-3,41546-29-6,41546-30-9,41546-31-0,126872-16-0,131064-98-7) + D-Fucose (73-34-7,87-96-7,488-79-9,551-63-3,609-01-8,643-17-4,643-18-5,4164-09-4,6014-42-2,6155-36-8,6189-71-5,6696-41-9,6736-43-2,13224-93-6,22611-09-2,28161-49-1,28161-50-4,28161-52-6,45864-36-6,63814-64-2,71116-59-1,71116-61-5,72598-05-1,87936-88-7,87936-89-8,97466-79-0,116908-82-8,120442-60-6,123484-22-0,133576-32-6) + polygalacic acid (22338-71-2)

Guidance literature:

With sulfuric acid; water; In 1,4-dioxane; for 1h; Reflux;

DOI:10.1007/s11418-016-0998-9

Reference yield:

(-)-lyoniresinol; 3α-O-β-D-xylopyranoside → beta-D-xylofuranoside (532-20-7,613-83-2,7261-25-8,7687-39-0,13221-22-2,14795-83-6,15761-67-8,20074-49-1,25545-03-3,25545-04-4,32445-75-3,34436-17-4,36441-93-7,36468-53-8,37388-49-1,38029-69-5,40461-77-6,40461-89-0,41546-19-4,41546-20-7,41546-21-8,41546-26-3,41546-29-6,41546-30-9,41546-31-0,126872-16-0,131064-98-7,37110-85-3) + (-)-(8S,8'S,7'S)-lyoniresinol (3737-93-7,14464-90-5,23212-64-8,73745-49-0,31768-94-2)

Guidance literature:

With hydrogenchloride;

DOI:10.1248/cpb.43.1937

Reference yield:

7-methylguanosine (20244-86-4) → 7-methylguanine (578-76-7) + D-Ribose (532-20-7,613-83-2,7261-25-8,7687-39-0,13221-22-2,14795-83-6,15761-67-8,20074-49-1,25545-03-3,25545-04-4,32445-75-3,34436-17-4,36441-93-7,36468-53-8,37110-85-3,37388-49-1,38029-69-5,40461-77-6,40461-89-0,41546-19-4,41546-20-7,41546-21-8,41546-26-3,41546-29-6,41546-30-9,41546-31-0,126872-16-0,131064-98-7)

Guidance literature:

With Caenorhabditis elegans group III nucleoside hydrolase C₄₂A mutant; water; sodium chloride; calcium chloride; In aq. buffer; at 25 ℃; pH=7.5; Concentration; Reagent/catalyst; Catalytic behavior; Kinetics; Enzymatic reaction;

DOI:10.1002/pro.3141

upstream raw materials:

3-O-α-L-rhamnopyranosyl(1->2)-α-L-arabinopyranosyl-oleanolic acid 28-O-β-D-xylopyranosyl(1->6)-β-D-glucopyranosyl ester

3-O-α-L-rhamnopyranosyl(1->2)-α-L-arabinopyranosyl-hederagenin 28-O-β-D-xylopyranosyl(1->6)-β-D-glucopyranosyl ester

adenine xyloside

tetra-O-acetyl-D-xylofuranose

Downstream raw materials:

2-amino-β-D-arabinofurano[1',2':4,5]-oxazoline

1,2-O-isopropylidene-α-D-xylofuranose-3,5-phenylboronate

O¹,O²;O³,O⁵-bis-phenylboranediyl-α-D-xylofuranose

(3aS,5R,6S,6aR)-2-<2,3,3a,5,6,6a-Hexahydro-6-hydroxy-5-(hydroxymethyl)furo<2,3-d>oxazol-2-yliden>cyanessigsaeure-methylester

Refernces

• 1、 Han, Qinghua,Qian, Yi,Wang, Xuda,Zhang, Qingying,Cui, Jingrong,Tu, Pengfei,Liang, Hong. "Oleanane-type saponins and prosapogenins from Albizia julibrissin and their cytotoxic activities". . . Retrieved 2021/04/02.
• 2、 Hao, Mimi,Ruan, Jingya,Sun, Fan,Wang, Tao,Wu, Lijie,Xiang, Guilin,Yan, Jiejing,Zhang, Yi,Zhang, Ying,Zhao, Wei. "New dammarane-type triterpenoid saponins from Panax notoginseng leaves and their nitric oxide inhibitory activities". . . Retrieved 2020/01/13.