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)-

(R)-Glycidyl 3-Nitrobenzenesulfonate

CAS: 115314-17-5

Formula: C₉H₉NO₆S

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 259.23

Ref: 3B-G0286

(R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate

CAS: 115314-17-5

Formula: C₉H₉NO₆S

Purity: 97%

Color and Shape: Solid

Molecular weight: 259.2359

Ref: IN-DA003C3E

(R)-Glycidyl nosylate

CAS: 115314-17-5

(R)-Glycidyl nosylate

Formula: C₉H₉NO₆S

Purity: 97%

Color and Shape: white solid

Molecular weight: 259.24g/mol

Ref: 54-OR315285

(R)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate

CAS: 115314-17-5

Formula: C₉H₉NO₆S

Purity: 97%

Color and Shape: Solid, White to slightly pale yellow crystal powder

Molecular weight: 259.23

Ref: 10-F212269

(R)-(-)-Glycidyl Nosylate

Controlled Product

CAS: 115314-17-5

Applications (R)-(-)-Glycidyl Nosylate (cas# 115314-17-5) is a compound useful in organic synthesis.

Formula: C₉H₉NO₆S

Color and Shape: Neat

Molecular weight: 259.24

Ref: TR-G615975

(R)-(-)-Glycidyl nosylate

CAS: 115314-17-5

(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: C₉H₉NO₆S

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 259.24 g/mol

Ref: 3D-FG23685