L-(+)Arabinose

• CAS: 87-72-9
• Catalog Number: ACM87729
• Category: Material of Health Food
• Molecular Weight: 150.13
• Molecular Formula: C5H10O5
• Description: 1.L-arabinose can be used as a sucrose enzyme inhibitor to lower the Glycaemic Index(GI) of sucrose containing products; 2.L-arabinose can be used in developing antiviral agents such as nucleoside analogues; 3.L-arabinose can be used in various foods (except foods for infants or young children); 4.L-arabinose can be used as raw material for the synthesis of fine chemicals as well as pharmaceutical intermediate; 5.L-arabinose can be used in preparing bacterial medium in biological industry; 6.L-arabinose can be used in the synthesis of flavours
• Appearance: White crystalline powder
• Effective Constituent: L-(+)Arabinose, arabinose

Custom Q&A

What is the molecular formula of L-(+)Arabinose?

The molecular formula of L-(+)Arabinose is C5H10O5.

What is the molecular weight of L-(+)Arabinose?

The molecular weight of L-(+)Arabinose is 150.13 g/mol.

What are some synonyms for L-(+)Arabinose?

Some synonyms for L-(+)Arabinose are beta-D-Arabinopyranose and (2R,3S,4R,5R)-oxane-2,3,4,5-tetrol.

Where is beta-D-Arabinopyranose found in nature?

Beta-D-Arabinopyranose is a natural product found in Psidium guajava, Pycnandra acuminata, and other organisms.

What is the InChI Key for L-(+)Arabinose?

The InChI Key for L-(+)Arabinose is SRBFZHDQGSBBOR-SQOUGZDYSA-N.

How many hydrogen bond donor counts does L-(+)Arabinose have?

L-(+)Arabinose has 4 hydrogen bond donor counts.

What is the XLogP3-AA value for L-(+)Arabinose?

The XLogP3-AA value for L-(+)Arabinose is -2.5.

What is the topological polar surface area of L-(+)Arabinose?

The topological polar surface area of L-(+)Arabinose is 90.2 Ų.

What is the formal charge of L-(+)Arabinose?

The formal charge of L-(+)Arabinose is 0.

What is the complexity value of L-(+)Arabinose?

The complexity value of L-(+)Arabinose is 117.

Synthetic Use

Downstream Synthesis Route 1

• 87-72-9
• 67-64-1

• 114861-22-2

Reference: [1] Tetrahedron Letters, 2014, vol. 55, # 2, p. 475 - 478

Downstream Synthesis Route 2

• 87-72-9
• 67-64-1

• 114861-22-2

Reference: [1] Patent: KR101770302, 2017, B1, . Location in patent: Paragraph 0331; 0332

Downstream Synthesis Route 3

• 87-72-9

• 114861-22-2

Reference: [1] Tetrahedron, 1988, vol. 44, # 15, p. 4721 - 4736

Downstream Synthesis Route 4

• 67-56-1
• 87-72-9

• 449173-64-2

Reference: [1]Current Patent Assignee: HE, SUI QING;LI, AI ZHEN;SHI, XIN JIAN;TONG, CHENG SONG;WANG, HAO - CN102153600, 2016, B
Location in patent: Paragraph 0254-0259
[2]Doares, Steven H.; Albersheim, Peter; Darvill, Alan G.
[Carbohydrate Research, 1991, vol. 210, p. 311 - 317]
[3]Tsuda; Kaneda; Yasufuku; Shimizu
[Chemical and Pharmaceutical Bulletin, 1981, vol. 29, # 8, p. 2123 - 2134]
[4]Motoki; Morita; Kobayashi; Uchida; Akimoto; Fukushima; Koezuka
[Biological and Pharmaceutical Bulletin, 1995, vol. 18, # 11, p. 1487 - 1491]
[5]Gutierrez, Marcelino; Capson, Todd L.; Guzman, Hector M.; Gonzalez, Jose; Ortega-Barria, Eduardo; Quinoa, Emilio; Riguera, Ricardo
[Journal of Natural Products, 2006, vol. 69, # 10, p. 1379 - 1383]

Downstream Synthesis Route 5

• 87-72-9
• 1124-32-9

• 2001-96-9

Reference: [1]Tetrahedron Letters,1994,vol. 35,p. 6279 - 6282

Downstream Synthesis Route 6

• 87-72-9

• 453-17-8
• 532-20-7
• 141-46-8
• 78-98-8

Reference: [1]Carbohydrate Research,1991,vol. 217,p. 71 - 86

* For details of the synthesis route, please refer to the original source to ensure accuracy.