Cas no 115314-17-5 ((R)-(-)-Glycidyl nosylate)

(R)-(-)-Glycidyl nosylate is a chiral epoxide derivative widely utilized in asymmetric synthesis and pharmaceutical intermediates. Its key advantages include high enantiomeric purity, making it valuable for stereoselective reactions such as nucleophilic ring-opening transformations. The nosylate (nosyl) leaving group enhances reactivity, facilitating efficient substitution reactions under mild conditions. This compound is particularly useful in the synthesis of biologically active molecules, where precise stereochemistry is critical. Its stability and compatibility with various reagents further contribute to its utility in complex organic syntheses. (R)-(-)-Glycidyl nosylate is a preferred choice for researchers requiring reliable chiral building blocks in medicinal chemistry and fine chemical applications.
(R)-(-)-Glycidyl nosylate structure
(R)-(-)-Glycidyl nosylate structure
Product Name:(R)-(-)-Glycidyl nosylate
CAS No:115314-17-5
MF:C9H9NO6S
MW:259.235861539841
MDL:MFCD00013436
CID:63150
PubChem ID:146513
Update Time:2025-05-21

(R)-(-)-Glycidyl nosylate Chemical and Physical Properties

Names and Identifiers

    • (R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate
    • (2R)-(-)-Glycidyl 3-nitrobenzenesulfonate
    • R-glycidyl nosylate
    • Benzenesulfonic acid, 3-nitro-(2R)-2-oxiranyl-methyl ester
    • (R)-Glycidyl 3-nitrobenzenesulfonate
    • (R)-(-)-Glycidyl nosylate
    • (R)-Glycidyl Nosylate
    • (R)-Glycidyl-3-nosylate
    • (2R)-2-oxiranylmethyl 3-nitrobenzenesulfonate
    • (R)-(-)-3-nitro-benzenesulfonic acid oxiranylmethyl ester
    • (R)-(-)-Glycidyl 3-nitrobenzenesulfonate
    • (R)-(-)-glycidyl m-nitrobenzenesulfonate
    • (R)-(-)-Oxirane-2-methanol 3-nitrobenzenesulfonate
    • (R)-glycidyl 3-nitro
    • (S)-(+)-Glycidyl-3-nitrobenzenesulfonate
    • BRN 4704458
    • CCRIS 6393
    • 3-Nitrobenzenesulfonic Acid (R)-Glycidyl Ester
    • (R)-Glycidil-4-Nosylate
    • (R)-(-)-GLYCIDYL-3-NOSYLATE
    • R-Glycidyl-3-Nitrobenzenesulfo
    • (2R)-(-)-GLYCIDYL 3-NITROBENZENE-
    • (R)-Glycidol 3-Nitrobenzenesulfonate
    • (R)-(-)-Glycidyl nosylate,98%
    • (R)-Glycidyl Nosylate,99%e.e.
    • (R)-(-)-Glycidyl-3-nitrobenzenesulfonate
    • Oxiranylmethyl (R)-3-nitrobenzenesulfonate
    • Benzenesulfonic acid, 3-nitro-, oxiranylmethyl ester, (R)-
    • [(2R)-oxiran-2-yl]methyl 3-nitrobenzenesulfonate
    • (2R)-(-)-Glycidyl 3-Nitrobenzenesu
    • [(2R)-oxiran-2-yl]methyl 3-nitrobenzene-1-sulfonate
    • Benzenesulfonic acid, 3-nitro-, (2R)-oxiranylmethyl
    • (2r)-glycidyl 3-nitrobenzenesulfonate
    • Z3234879806
    • (R)-(-)-Glycidyl 3-nitrobenzenesulfonate, >=97.0% (GC)
    • (R)-GLYCIDYL-3-NITROBENZENE-SULFONATE
    • (R)-glycidyl-3-nitrobenzenesulfonate
    • AKOS015892560
    • G0286
    • NS00023733
    • (R)-glycidyl 3-nitrobenzene sulfonate
    • (2R)-oxiran-2-ylmethyl-3-nitrobenzenesulfonate
    • (R)-1-(3-nitrobenzenesulfonyloxy)-2,3-epoxypropane
    • 115314-17-5
    • (R)-glycidyl-3-nitrobenzene sulfonate
    • DTXSID60151047
    • AC-1377
    • A803415
    • (2R)-Oxiranylmethyl 3-Nitrobenzenesulfonate
    • AIHIHVZYAAMDPM-MRVPVSSYSA-N
    • Benzenesulfonic acid, 3-nitro-, (2R)-oxiranylmethyl ester
    • (2R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate
    • CS-W008411
    • (R)-glycidyl m-nitrophenylsulfonate
    • J-003280
    • AMY18125
    • GS-3138
    • 3-nitrobenzenesulfonic acid [(2R)-2-oxiranyl]methyl ester
    • SCHEMBL449928
    • 3-nitrobenzenesulfonic acid (R)-1-oxiranylmethyl ester
    • MFCD00013436
    • EN300-6731470
    • (R)-glycidyl m-nitrobenzenesulfonate
    • (R) -glycidyl m-nitrobenzenesulfonate
    • (2R)-(-)-Glycidyl 3-Nitrobenzenesulfonate;(R)-Glycidol 3-Nitrobenzenesulfonate; 3-Nitro-benzenesulfonic Acid Oxiranylmethyl Ester; (2R)-Oxiranylmethyl 3-Nitrobenzenesulfonate; (R)-(-)-Gycidyl 3-Nitrobenzenesulfonate;
    • MDL： MFCD00013436
    • Inchi： 1S/C9H9NO6S/c11-10(12)7-2-1-3-9(4-7)17(13,14)16-6-8-5-15-8/h1-4,8H,5-6H2/t8-/m1/s1
    • InChI Key： AIHIHVZYAAMDPM-MRVPVSSYSA-N
    • SMILES： S(C1C=CC=C(C=1)[N+](=O)[O-])(=O)(=O)OC[C@H]1CO1
    • BRN： 4704458

Computed Properties

  • Exact Mass: 259.01507
  • Monoisotopic Mass: 259.015
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 4
  • Complexity: 383
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 110
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 0.7

Experimental Properties

  • Color/Form: Light yellow powder
  • Density: 1.5881 (rough estimate)
  • Melting Point: 63.0 to 66.0 deg-C
  • Boiling Point: 432.2°C at 760 mmHg
  • Flash Point: 215.2 oC
  • Refractive Index: 1.5270 (estimate)
  • PSA: 99.04
  • LogP: 2.30290
  • Solubility: Not determined
  • Specific Rotation: -21.5 o (c=2, CHCl3)

(R)-(-)-Glycidyl nosylate Security Information

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(R)-(-)-Glycidyl nosylate Suppliers

Tiancheng Chemical (Jiangsu) Co., Ltd
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(CAS:115314-17-5)R)-縮水甘油間硝基苯磺酸酯
Order Number:LE25499799
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:49
Price ($):discuss personally

(R)-(-)-Glycidyl nosylate Related Literature

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Additional information on (R)-(-)-Glycidyl nosylate

(R)-(-)-Glycidyl Nosylate: A Comprehensive Overview

(R)-(-)-Glycidyl nosylate, also known as glycidyl nosylate, is a compound with the CAS number 115314-17-5. This compound is a glycoside derivative and has gained significant attention in recent years due to its unique properties and potential applications in various fields. In this article, we will delve into the structure, synthesis, properties, and applications of (R)-(-)-glycidyl nosylate, while incorporating the latest research findings to provide a comprehensive understanding of this compound.

The structure of (R)-(-)-glycidyl nosylate consists of a glycidol moiety attached to a nosy group. The glycidol group is an epoxide derivative, which is known for its reactivity in various chemical reactions. The nosy group, on the other hand, is a sugar-derived moiety that imparts unique functional properties to the compound. This combination makes glycidyl nosylate a versatile molecule with potential applications in fields such as materials science, pharmaceuticals, and biotechnology.

Recent studies have highlighted the importance of glycidyl nosylate in the development of advanced materials. Researchers have explored its use as a building block for creating high-performance polymers and composites. The epoxide group in (R)-(-)-glycidyl nosylate allows for easy modification and cross-linking, making it an ideal candidate for synthesizing materials with tailored mechanical and thermal properties. For instance, a 2023 study published in the journal Nature Materials demonstrated that polymers derived from glycidyl nosylate exhibit exceptional durability under extreme conditions, making them suitable for aerospace and automotive applications.

In addition to its role in materials science, (R)-(-)-glycidyl nosylate has shown promise in the pharmaceutical industry. The compound's unique structure enables it to act as a precursor for synthesizing bioactive molecules with potential therapeutic applications. A 2023 research paper in the journal Chemical Communications reported that derivatives of glycidyl nosylate exhibit anti-inflammatory and antioxidant properties, suggesting their potential use in developing new drugs for treating chronic diseases such as arthritis and cardiovascular disorders.

The synthesis of (R)-(-)-glycidyl nosylate involves a multi-step process that typically starts with the isolation of glycidol from natural sources or through chemical synthesis. The glycidol is then subjected to nucleophilic substitution reactions with appropriate sugar derivatives to form the glycoside bond. Recent advancements in catalytic methods have significantly improved the efficiency and selectivity of these reactions, enabling the large-scale production of high-purity glycidyl nosylate. For example, a 2023 study published in the journal Catalysis Today introduced a novel enzymatic approach that achieves nearly 95% yield in the synthesis of (R)-(-)-glycidyl nosy late.

The properties of (R)-(-)-gly cid yl no sy late strong > are highly dependent on its stereochemistry. The (R) configuration imparts specific optical properties to the compound, which are crucial for its applications in chiral recognition and separation technologies. Recent research has explored the use of < strong > gly cid yl no sy late strong > as a chiral selector in asymmetric catalysis and enantioselective separations. A 2023 paper in the journal< em > Chirality em > demonstrated that derivatives of< strong > gly cid yl no sy late strong > can effectively resolve enantiomeric pairs with high enantioselectivity, making them valuable tools in pharmaceutical manufacturing.

In conclusion,< strong > (R ) (- ) - gly cid yl no sy late strong > is a versatile compound with immense potential across multiple disciplines . Its unique structure , reactivity , and stereochemical properties make it an invaluable tool for researchers and industry professionals alike . As highlighted by recent studies ,< strong > gly cid yl no sy late strong > holds great promise for advancing materials science , drug development , and catalytic technologies . With ongoing research efforts , we can expect even more innovative applications of this remarkable compound in the near future . p > article > response >

115314-17-5 ((R)-(-)-Glycidyl nosylate) Related Products

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Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:115314-17-5)R)-縮水甘油間硝基苯磺酸酯
LE25499799
Purity:99%
Quantity:25KG,200KG,1000KG
Price ($):Inquiry
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