beta-D-Ribofuranose 1,2,3,5-tetraacetate

Base Information

  • PRODUCT:beta-D-Ribofuranose 1,2,3,5-tetraacetate
  • CAS.:13035-61-5
  • MF:C13H18O9
  • Molecular Weight:318.281
  • Purity:99%

Product Details

CAS： 13035-61-5

MF： C13H18O9

Appearance： white to almost white crystalline powder

Chinese Manufacturer supply beta-D-Ribofuranose 1,2,3,5-tetraacetate 13035-61-5 in stock with high standard

  • Molecular Formula:C13H18O9
  • Molecular Weight:318.281
  • Appearance/Colour:white to almost white crystalline powder 
  • Vapor Pressure:3.76E-06mmHg at 25°C 
  • Melting Point:81-83 °C(lit.) 
  • Refractive Index:-14.5 ° (C=5, MeOH) 
  • Boiling Point:385.6 °C at 760 mmHg 
  • Flash Point:168.5 °C 
  • PSA：114.43000 
  • Density:1.29 g/cm3 
  • LogP:-0.29910 

beta-D-Ribofuranose 1,2,3,5-tetraacetate(Cas 13035-61-5) Usage

Nucleotides: Precursor in the synthesis of nucleotides, which have antiproliferative activity against cancer cells.
Nucleosides: Starting material for the synthesis of nucleosides.
Ribosylations: Used in ribosylation reactions.
Hazards: Can cause skin and eye irritation, and may irritate the respiratory system.
Skin Contact: Wash immediately with soap and water, and remove any contaminated clothing or shoes.

InChI:InChI=1/C13H18O9/c1-6(14)18-5-10-11(19-7(2)15)12(20-8(3)16)13(22-10)21-9(4)17/h10-13H,5H2,1-4H3/t10-,11?,12?,13-/m1/s1

Hebei KuiSheng Trading Co., LTD ，a company specializing in the production and supply of chemicals for various industries. we take pride in our ability to carefully formulate chemicals that meet the highest standards of quality, efficiency, and safety. Through advanced technology and strict quality control measures, we ensure that our products consistently deliver exceptional performance and reliability. Whether you are in need of chemicals for pharmaceutical, agricultural, or industrial applications, we offer a wide range of solutions to meet your specific requirements. Our team is dedicated to providing excellent customer service and we strongly believe in establishing long-lasting business relationships built on trust and mutual success. Allow me to outline some of our key advantages: 1. High quality with competitive prices: We strive to offer chemicals of the highest quality while remaining competitive in the market. 2. All purity >99%: Our products undergo rigorous purification processes to guarantee high purity levels. 3. Manufacturer with factory prices: As a manufacturer, we have the ability to offer high-quality products at competitive factory prices. 4. Fast and safe delivery: We understand the importance of timely and secure deliveries. Therefore, we have established reliable logistics networks to ensure efficient transportation of our products. 5. OEM is welcome: We are open to providing Original Equipment Manufacturer (OEM) services, allowing you to customize products according to your specific needs. 6. Sufficient stock: Our extensive inventory ensures that we can fulfill orders promptly, regardless of their size or complexity. We are confident that with our extensive experience and dedication to excellence, we can be your trusted partner in chemical solutions. We would greatly appreciate the opportunity to work with you and contribute to the success of your business. Should you require any further information or have specific inquiries, please do not hesitate to contact us. We look forward to hearing from you.

13035-61-5 Relevant articles

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The potent and selective antiviral drug ...

Syntheses of 1-thio-D-xylose and D-ribose esters of diorganoarsinous acids and their anticancer activity

Gao, Mingzhang,Chen, Yiwen,Tan, Songde,Reibenspies, Joseph H.,Zingaro, Ralph A.

, p. 199 - 206 (2008)

Several thio-D-xylose and D-ribose ester...

Synthesis and antiviral evaluation of nucleoside analogues bearing one pyrimidine moiety and two d-ribofuranosyl residues

Andreeva, Olga V.,Belenok, Mayya G.,Garifullin, Bulat F.,Kataev, Vladimir E.,Lyubina, Anna P.,Man’kova, Maria A.,Saifina, Liliya F.,Semenov, Vyacheslav E.,Shulaeva, Marina M.,Slita, Alexander V.,Volobueva, Alexandrina S.,Voloshina, Alexandra D.,Yesaulkova, Iana L.,Zarubaev, Vladimir V.

, (2021/07/06)

A series of 1,2,3-triazolyl nucleoside a...

Glycosides and Glycoconjugates of the Diterpenoid Isosteviol with a 1,2,3-Triazolyl Moiety: Synthesis and Cytotoxicity Evaluation

Andreeva, Olga V.,Garifullin, Bulat F.,Sharipova, Radmila R.,Strobykina, Irina Yu.,Sapunova, Anastasiya S.,Voloshina, Alexandra D.,Belenok, Mayya G.,Dobrynin, Alexey B.,Khabibulina, Leysan R.,Kataev, Vladimir E.

, p. 2367 - 2380 (2020/08/28)

Several glycoconjugates of the diterpeno...

13035-61-5 Process route

acetic anhydride
108-24-7

acetic anhydride

G
118-00-3

G

2,9-diacetylguanine
3056-33-5

2,9-diacetylguanine

1,2,3,5-tetraacetylribose
13035-61-5

1,2,3,5-tetraacetylribose

Conditions
Conditions Yield
acetic anhydride; G; at 136 ℃; for 1h;
With trifluoroacetic acid; at 60 - 100 ℃;
86%
96%
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

L-(+)-arabinose

acetic anhydride
108-24-7

acetic anhydride

1,2,3,6-tetra-O-acetyl-5-deoxy-α-L-arabino-hexofuranose
13035-61-5,23094-61-3,28708-32-9,39727-26-9,42927-46-8,43225-70-3,50730-26-2,56272-01-6,61248-15-5,61826-42-4,61849-90-9,69855-18-1,69855-19-2,79120-80-2,79120-81-3,86782-36-7,86782-94-7,105453-36-9,144490-03-9

1,2,3,6-tetra-O-acetyl-5-deoxy-α-L-arabino-hexofuranose

1,2,3,6-tetra-O-acetyl-5-deoxy-β-L-arabino-hexofuranose
13035-61-5,23094-61-3,28708-32-9,39727-26-9,42927-46-8,43225-70-3,50730-26-2,56272-01-6,61248-15-5,61826-42-4,61849-90-9,69855-18-1,69855-19-2,79120-80-2,79120-81-3,86782-36-7,86782-94-7,105453-36-9,144490-03-9

1,2,3,6-tetra-O-acetyl-5-deoxy-β-L-arabino-hexofuranose

1,2,3,4-tetra-O-acetyl-β-L-arabinopyranose
4258-00-8

1,2,3,4-tetra-O-acetyl-β-L-arabinopyranose

1,2,3,4-tetra-O-acetyl-α-L-arabinopyranose
1233-03-0,2595-11-1,4026-34-0,4049-33-6,4049-34-7,4257-95-8,4257-98-1,4258-00-8,4627-30-9,17080-99-8,19186-37-9,25227-11-6,25243-38-3,62446-93-9,62929-49-1,67226-03-3,78087-60-2,78088-17-2,82890-16-2,86782-34-5,86782-35-6,92218-63-8,99880-95-2,108646-05-5,115939-79-2,123163-97-3,142130-89-0

1,2,3,4-tetra-O-acetyl-α-L-arabinopyranose

Conditions
Conditions Yield
With pyridine; at 0 ℃; Yield given. Yields of byproduct given;
 
With H-Beta zeolite; for 2h; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature;
 
With sodium acetate; Yield given. Yields of byproduct given;
 
With pyridine; N,N-dimethyl-formamide; at 120 ℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
 
With sodium acetate; Product distribution; other reagent, other temperature;
 
With pyridine; at 25 ℃; for 12h; Reagent/catalyst; Overall yield = 100 %; Overall yield = 11.11 g; stereoselective reaction; Inert atmosphere;
20 % de
20 % de

13035-61-5 Upstream products

  • 94482-37-8
    94482-37-8

    5-O-triphenylmethyl-D-ribofuranose-1,2,3-triacetate

  • 506-96-7
    506-96-7

    Acetyl bromide

  • 108-24-7
    108-24-7

    acetic anhydride

  • 110-86-1
    110-86-1

    pyridine

13035-61-5 Downstream products

  • 2140-61-6
    2140-61-6

    4-amino-5-methyl-1-α-D-ribofuranosyl-1H-pyrimidin-2-one

  • 86480-36-6
    86480-36-6

    3-β-D-ribofuranosyl-5-(methylthio)-3H-1,2,3-triazolo<4,5-d>pyrimidin-7-amine

  • 86480-42-4
    86480-42-4

    (2R,3R,4S,5R)-2-(7-Amino-5-methylsulfanyl-[1,2,3]triazolo[4,5-d]pyrimidin-2-yl)-5-hydroxymethyl-tetrahydro-furan-3,4-diol

  • 86480-43-5
    86480-43-5

    (2R,3R,4S,5R)-2-(7-Amino-5-methanesulfonyl-[1,2,3]triazolo[4,5-d]pyrimidin-2-yl)-5-hydroxymethyl-tetrahydro-furan-3,4-diol

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