Cas no 4630-62-0 (Phenyl a-D-Glucopyranoside)

Phenyl α-D-Glucopyranoside is a synthetic glycoside derivative in which a phenyl group is linked to the anomeric carbon of α-D-glucopyranose via a glycosidic bond. This compound is widely utilized in biochemical and enzymatic studies, particularly as a substrate for glycosidase enzymes, including α-glucosidases, to investigate catalytic mechanisms and enzyme specificity. Its stable glycosidic linkage and well-defined structure make it a valuable tool for probing carbohydrate-active enzymes. Additionally, it serves as a precursor in the synthesis of more complex glycoconjugates. The compound’s purity and consistency ensure reliable performance in research applications, supporting studies in glycobiology and enzymology.
Phenyl a-D-Glucopyranoside structure
Phenyl a-D-Glucopyranoside structure
Product Name:Phenyl a-D-Glucopyranoside
CAS No:4630-62-0
MF:C12H16O6
MW:256.251844406128
MDL:MFCD00006594
CID:330549
PubChem ID:87575433
Update Time:2025-10-31

Phenyl a-D-Glucopyranoside Chemical and Physical Properties

Names and Identifiers

    • a-D-Glucopyranoside, phenyl
    • Phenyl α-D-Glucopyranoside
    • Phenyl Alpha-D-Glucoside
    • Phenyl alpha-D-Glucopyranoside
    • (3S,4S,6R)-2-(hydroxymethyl)-6-phenoxyoxane-3,4,5-triol
    • Phenyl α-D-Glucopyra
    • PHENYL-A-D-GLUCOPYRANOSIDE(RG)
    • -<small>D<
    • Brn 0087520
    • Nsc 226967
    • PHENYL A-D-GLUCOPYRANOSIDE
    • PHENYL-A-D-GLUCOSIDE
    • Phenyl α-D-Glucoside
    • Phenyl a-D-Glucopyranoside
    • MDL: MFCD00006594
    • Inchi: 1S/C12H16O6/c13-6-8-9(14)10(15)11(16)12(18-8)17-7-4-2-1-3-5-7/h1-5,8-16H,6H2/t8-,9-,10+,11-,12+/m1/s1
    • InChI Key: NEZJDVYDSZTRFS-ZIQFBCGOSA-N
    • SMILES: O1[C@@H]([C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O)OC1C=CC=CC=1

Computed Properties

  • Exact Mass: 1461.99462
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 3
  • Complexity: 255
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 5
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • XLogP3: -0.9
  • Topological Polar Surface Area: 99.4

Experimental Properties

  • Color/Form: Uncertain
  • Melting Point: 171.0 to 175.0 deg-C
  • Refractive Index: 180 ° (C=1, H2O)
  • PSA: 92.3
  • LogP: -1.13470
  • Solubility: Uncertain

Phenyl a-D-Glucopyranoside Security Information

  • WGK Germany:3
  • Hazard Category Code: 34
  • Safety Instruction: 26-27-36/37/39-45
  • Regulatory Condition Code:Class Q (sugars, alkaloids, antibiotics, hormones)
  • RTECS:LZ5985500
  • Hazardous Material Identification: C
  • Storage Condition:<0°C
  • Risk Phrases:34

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Phenyl a-D-Glucopyranoside Suppliers

Amadis Chemical Company Limited
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(CAS:4630-62-0)Phenyl a-D-Glucopyranoside
Order Number:A1205269
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 15:57
Price ($):309.0

Phenyl a-D-Glucopyranoside Related Literature

Additional information on Phenyl a-D-Glucopyranoside

Phenyl a-D-Glucopyranoside (CAS No. 4630-62-0): A Comprehensive Guide to Its Properties and Applications

Phenyl a-D-Glucopyranoside (CAS No. 4630-62-0) is a glycoside compound widely studied in biochemistry and pharmaceutical research. This aromatic glucoside is derived from the conjugation of glucose with a phenyl group, making it a valuable tool for enzymatic studies and carbohydrate metabolism research. Its unique structure, featuring an a-D-glucopyranosyl moiety, has garnered attention in fields like glycobiology and drug development.

In recent years, the demand for Phenyl a-D-Glucopyranoside has surged due to its role in understanding enzyme-substrate interactions, particularly in glycosidase assays. Researchers frequently search for "Phenyl a-D-Glucopyranoside uses" or "CAS 4630-62-0 solubility," reflecting its relevance in lab protocols. The compound’s stability in aqueous solutions and compatibility with high-throughput screening systems make it a preferred choice for studying diabetes-related enzymes like alpha-glucosidase.

The synthesis of Phenyl a-D-Glucopyranoside involves stereoselective glycosylation, a topic often queried as "how to synthesize phenyl glucosides." Its crystalline form and melting point (typically ~180°C) are critical for purity verification, a common concern among purchasers. Additionally, its non-toxic profile aligns with the growing trend toward green chemistry, addressing queries like "eco-friendly glycosides."

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In summary, Phenyl a-D-Glucopyranoside bridges fundamental science and industrial innovation. Its versatility in biocatalysis, coupled with rising interest in functional carbohydrates, ensures its prominence in both literature and search engine trends.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:4630-62-0)Phenyl a-D-Glucopyranoside
A1205269
Purity:99%
Quantity:1g
Price ($):309.0
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