beta-D-Arabinopyranose (9CI)

Base Information

• Chemical Name: beta-D-Arabinopyranose (9CI)
• CAS No.: 6748-95-4
• Molecular Formula: C5H10O5
• Molecular Weight: 150.1299
• Hs Code.: 2932999099
• Mol file: 6748-95-4.mol

Synonyms:D-xylose;β-D-Arabinopyranose;

Chemical Property of beta-D-Arabinopyranose (9CI)

Chemical Property:

• Melting Point: 155.5°C
• Refractive Index: 1.3920 (estimate)
• Boiling Point: 191.65°C (rough estimate)
• PSA: 90.15000
• Density: 1.6250
• LogP: -2.58230

Purity/Quality:

98%, ^*data from raw suppliers

(2R,3S,4R,5R)-oxane-2,3,4,5-tetrol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of beta-D-Arabinopyranose (9CI)

There total 714 articles about beta-D-Arabinopyranose (9CI) 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:

jujuboside B (Compound I) (55466-05-2,68144-21-8,77943-54-5) → 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) + 3-O-<α-L-Rhamnopyranosyl-(1->2)-<β-D-glucopyranosyl-(1->3)>-α-L-arabinopyranosyl>jujubogenin (77174-32-4,77943-56-7,77943-83-0,146503-30-2)

Guidance literature:

With hesperidinase; Tween 80; In ethanol; water; at 37 ℃; for 72h;

DOI:10.1248/cpb.29.676

Reference yield:

jujuboside B (Compound I) (55466-05-2,68144-21-8,77943-54-5) → D-Glucose (2280-44-6) + ebelin lactone (3649-76-1) + L-rhamnose (73-34-7) + L-(+)-arabinose (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)

Guidance literature:

With sulfuric acid; In ethanol; water; for 2h; Further byproducts given; Heating;

DOI:10.1248/cpb.29.676

Reference yield:

Zizyphus saponin III (55466-05-2,68144-21-8,77943-54-5) → 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) + Zizyphus saponin I (77174-32-4,77943-56-7,77943-83-0,146503-30-2)

Guidance literature:

With hesperidinase; In water; at 37 ℃; for 96h;

DOI:10.1248/cpb.29.676

upstream raw materials:

diazomethane

3-O-β-D-galactopyranosyl-(1->2)-<β-D-xylopyranosyl-(1->3)>-β-D-glucuronopyranosyl quillaic acid 28-O-β-D-apiofuranosyl-(1->3)-β-D-xylopyranosyl-(1->4)-<β-D-glucopyranosyl-(1->3)>-α-L-rhamnopyranosyl-(1->2)-β-D-fucopyranoside.

methanol

D-(+)-xylobiose

Downstream raw materials:

methyl xyloside

methyl-β-D-xylopyranoside

methyl-α-D-xylopyranoside

5-deoxy-1,2-O-isopropylidene-α-D-xylohexofuranose

Refernces

• 1、 Jiang, Pei-Jing,Lu, Mei-Jiao,Xi, Yi-Yuan,Chen, Jun,Zheng, Ju-Jia,Xu, Xiang-Wei. "New flavonoid glycosides from Xanthium strumarium with their protein tyrosine phosphatase 1B inhibitory activity". . p. 45 - 51. Retrieved 2021/01/25.
• 2、 Li, Yao-Lan,Li, Ying-Ying,Tang, Qing,Wang, Guo-Cai,Wang, Wen-Zhi,Wu, Zhong-Nan,Zhan, Zhao-Chun,Zhang, Sheng-Yuan,Zhang, Yu-Bo. "Stilbene dimer xylosides and flavanols from the roots of Lysidice rhodostegia and their antioxidant activities". . . Retrieved 2021/08/03.