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3,3-dimethyl-2-(propan-2-yl)oxaziridine is a chemical compound with the molecular formula C7H15NO. It is a cyclic amine derivative, specifically an oxaziridine, which is characterized by the presence of a three-membered ring containing one nitrogen and two oxygen atoms. The compound features two methyl groups (-CH3) attached to the carbon adjacent to the nitrogen atom, and a propyl group (-C3H7) attached to the carbon opposite the nitrogen atom. This structure endows the compound with unique reactivity and properties, making it a potentially useful intermediate in organic synthesis. It is important to note that the compound's reactivity and potential applications may vary depending on the specific context and conditions in which it is used.

2763-77-1

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2763-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2763-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2763-77:
(6*2)+(5*7)+(4*6)+(3*3)+(2*7)+(1*7)=101
101 % 10 = 1
So 2763-77-1 is a valid CAS Registry Number.

2763-77-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyl-2-propan-2-yloxaziridine

1.2 Other means of identification

Product number -
Other names 3,3-Dimethyl-2-isopropyl-oxaziridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2763-77-1 SDS

2763-77-1Downstream Products

2763-77-1Relevant academic research and scientific papers

Photochemistry and Photophysics of Small Heterocyclic Molecules: 1. Multiphoton Ionization and Dissociation of N-Isopropyldimethyloxaziridine

Michelsen, H. A.,Giugliano, R. P.,BelBruno, J. J.

, p. 3034 - 3039 (1985)

The resonantly enhanced visible multiphoton ionization spectrum of N-isopropyldimethyloxaziridine has been recovered over the wavelength region from 375 to 600 nm.Rydberg series have been observed and assigned to ns, np, and nd transitions, with n spanning the range from 3 to 6.These transitions are accompanied by changes in the vibrational energy of a ring deformation mode.The ionization potential for this molecule is estimated to be 8.84 eV from both the Rydberg series limits and the spectral changes accompanying the transitions from a three- to a four-photon requirement for ionization.Preliminary gas-phase photochemical results indicate a sharp energy dependence in the mechanism for dissociation.A one-photon pathway leads primarily to simple ring opening and an amide final product, while a second, multiphoton channel leads exclusively to the severing of two bonds and an acetone fragment.These results are compared with earlier theoretical predictions and experimental results.The unique advantages of multiphoton photochemistry for the production of novel species are discussed.

Sulfonic peracids - III. Heteroatom oxidation and chemoselectivity

Kluge,Schulz,Liebsch

, p. 5773 - 5782 (2007/10/03)

We have investigated the p-toluenesulfonic peracid (2) generated in situ in the oxidation of different types of compounds containing nitrogen and/or sulfur. The sulfonic peracid 2 shows a remarkable chemoselectivity characterized by a preferred oxidation of sulfides to the sulfones in the presence of amines or olefins and a strong dependence on the nature of the amine in the competitive oxidation of olefins and amines.

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