CAS 36016-39-4

[(1,1-Dimethylethoxy)carbonyl]azanyl 2,4,6-trimethylbenzenesulfonate

Description:

The chemical substance known as "[(1,1-Dimethylethoxy)carbonyl]azanyl 2,4,6-trimethylbenzenesulfonate," with the CAS number 36016-39-4, is a sulfonate compound characterized by the presence of a sulfonic acid group attached to a trimethyl-substituted aromatic ring. This compound features a carbonyl group linked to a dimethylethoxy moiety, which contributes to its stability and solubility in organic solvents. The azanyl (amine) group indicates the presence of nitrogen, which can participate in various chemical reactions, including nucleophilic substitutions. The trimethyl groups on the benzene ring enhance the steric bulk and influence the compound's reactivity and interaction with other molecules. This compound may exhibit properties such as moderate polarity, making it suitable for applications in organic synthesis, pharmaceuticals, or as a reagent in chemical reactions. Its specific characteristics, including melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which it is studied.

Formula: C₁₄H₂₁NO₅S

InChI: InChI=1/C14H21NO5S/c1-9-7-10(2)12(11(3)8-9)21(17,18)20-15-13(16)19-14(4,5)6/h7-8H,1-6H3,(H,15,16)

InChI key: InChIKey=WVMDSNGINQNHLN-UHFFFAOYSA-N

SMILES: S(ONC(OC(C)(C)C)=O)(=O)(=O)C1=C(C)C=C(C)C=C1C

Synonyms:

• 1,1-Dimethylethyl [[(2,4,6-trimethylphenyl)sulfonyl]oxy]carbamate
• Benzenesulfonic acid, 2,4,6-trimethyl-, [(1,1-dimethylethoxy)carbonyl]azanyl ester
• Carbamic acid, [[(2,4,6-trimethylphenyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester
• Carbamic acid, hydroxy-, tert-butyl ester, 2-mesitylenesulfonate
• N-Boc-O-(Mesitylsulfonyl)Hydroxylamine
• N-tert-Butoxycarbonyl-O-(mesitylsulfonyl)hydroxylamine
• NSC 620029
• Tert-Butyl {[(2,4,6-Trimethylphenyl)Sulfonyl]Oxy}Carbamate
• [(1,1-Dimethylethoxy)carbonyl]azanyl 2,4,6-trimethylbenzenesulfonate
• [(2-Methylpropan-2-yl)oxycarbonylamino] 2,4,6-trimethylbenzenesulfonate
• tert-Butyl (((mesityl)sulfonyl)oxy)carbamate
• 1-dimethylethyl [[(2,4,6-trimethylphenyl)sulphonyl]oxy]carbamate
• 1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamate
• _x000D_N-Boc-O-(mesitylsulfonyl)hydroxylamine
• N-[[(2,4,6-Trimethylphenyl)sulfonyl]oxy]carbamic acid tert-butyl ester
• N-Boc-O-(mesitylsulfonyl)hydroxyamine
• N-Mesitylsulfonyloxy-tert-butylcarbaMat
• tert-butyl N-[(2,4,6-trimethylbenzenesulfonyl)oxy]carbamate
• tert-Butyl (Mesitylsulfonyl)oxycarbaMate

N-tert-Butoxycarbonyl-O-(mesitylsulfonyl)hydroxylamine

CAS: 36016-39-4

N-tert-Butoxycarbonyl-O-(mesitylsulfonyl)hydroxylamine

Formula: C₁₄H₂₁NO₅S

Purity: 99%

Color and Shape: white solid

Molecular weight: 315.39g/mol

Ref: 54-OR906655

tert-Butyl (mesitylsulfonyl)oxycarbamate

CAS: 36016-39-4

Formula: C₁₄H₂₁NO₅S

Purity: 95%

Color and Shape: Solid

Molecular weight: 315.38

Ref: 10-F213311

tert-Butyl (((Mesityl)sulfonyl)oxy)carbamate

Controlled Product

CAS: 36016-39-4

Stability Hygroscopic
Applications tert-Butyl (((mesityl)sulfonyl)oxy)carbamate is a useful reagent for the enantioselective aziridination of α,β-unsaturated aldehydes.
References Arai, H., et l.: Tetrahedron Lett., 50, 3329(2009)

Formula: C₁₄H₂₁NO₅S

Color and Shape: Neat

Molecular weight: 315.39

Ref: TR-B163940

N-Boc-O-(mesitylsulfonyl)hydroxylamine

CAS: 36016-39-4

Formula: C₁₄H₂₁NO₅S

Color and Shape: Solid

Molecular weight: 315.3852

Ref: IN-DA0035D5