CAS 115314-17-5
:Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl ester
Description:
Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl ester, identified by CAS number 115314-17-5, is an organic compound characterized by its sulfonic acid and nitro functional groups, along with an epoxide moiety. This compound typically exhibits a polar nature due to the presence of the sulfonic acid group, which enhances its solubility in polar solvents. The nitro group contributes to its reactivity, making it a potential candidate for electrophilic substitution reactions. The epoxide structure indicates the presence of a three-membered cyclic ether, which is known for its strain and reactivity, particularly in nucleophilic ring-opening reactions. This compound may be utilized in various chemical syntheses and applications, including pharmaceuticals and agrochemicals, due to its functional versatility. Additionally, its stability under standard conditions allows for handling and storage, although care should be taken due to the potential reactivity of the nitro and epoxide groups. Overall, this compound represents a unique combination of functional groups that can be leveraged in synthetic organic chemistry.
Formula:C9H9NO6S
InChI: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:InChIKey=AIHIHVZYAAMDPM-MRVPVSSYSA-N
SMILES:S(OC[C@H]1CO1)(=O)(=O)C2=CC(N(=O)=O)=CC=C2
Synonyms:- ((2R)-Oxiran-2-yl)methyl 3-nitrobenzenesulfonate
- (2R)-(-)-Glycidyl 3-nitrobenzenesulfonate
- (R)-(-)-3-Nitrobenzenesulfonic acid oxiranylmethyl ester
- (R)-(-)-Glycidyl-3-Nitrobenzenesulfonate
- (R)-(-)-Oxiran-2-ylmethyl-3-nitrobenzenesulfonate
- (R)-(2,3-Epoxypropan-1-yl) 3-nitrobenzenesulfonate
- (R)-2,3-Epoxypropyl 3-nitrobenzenesulfonate
- (R)-3-nitrobenzenesulfonic acid glycidyl ester
- 3-Nitrobenzenesulfonic acid (R)-glycidyl ester
- 3-Nitrobenzenesulfonic acid (R)-oxiran-2-ylmethyl ester
- 3-Nitrobenzensulfonic acid (R)-oxiran-2-ylmethyl ester
- Benzenesulfonic acid, 3-nitro-(2R)-2-oxiranyl-methyl ester
- Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl ester
- Benzenesulfonic acid, 3-nitro-, (2R)-oxiranylmethyl ester
- Benzenesulfonic acid, 3-nitro-, oxiranylmethyl ester, (R)-
- See more synonyms
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Found 7 products.
(R)-Glycidyl 3-Nitrobenzenesulfonate
CAS:Formula:C9H9NO6SPurity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:259.23(R)-Glycidyl nosylate
CAS:(R)-Glycidyl nosylateFormula:C9H9NO6SPurity:97%Color and Shape:Light yellow Solid-PowderMolecular weight:259.23586(R)-(-)-Glycidyl Nosylate
CAS:(R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonateFormula:C9H9NO6SPurity:97%Molecular weight:259.24(R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate
CAS:Formula:C9H9NO6SPurity:97%Color and Shape:Solid, White to slightly pale yellow crystal powderMolecular weight:259.23(R)-(-)-Glycidyl Nosylate
CAS:Controlled ProductApplications (R)-(-)-Glycidyl Nosylate (cas# 115314-17-5) is a compound useful in organic synthesis.
Formula:C9H9NO6SColor and Shape:NeatMolecular weight:259.24(R)-(-)-Glycidyl nosylate
CAS:(R)-(-)-Glycidyl nosylate is an epoxide that is used in the synthesis of pharmaceuticals. It has shown mutagenic activity and can be used to produce chiral glycidyl compounds. (R)-(-)-Glycidyl nosylate has been evaluated as a potential drug for the treatment of cancer, but was found to have limited pharmacological activity. This compound binds to protein kinases and may inhibit their activity. (R)-(-)-Glycidyl nosylate also possesses aliphatic properties and is an enantiopure molecule. The stereoisomers of glycidyl nosylate are also available, with the most common being (+)glycidylether.
Formula:C9H9NO6SPurity:Min. 95%Color and Shape:White PowderMolecular weight:259.24 g/mol(R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate
CAS:Formula:C9H9NO6SPurity:97%Color and Shape:SolidMolecular weight:259.2359
