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2-Oxazolidinone, 3-benzoyl-5-methyl- is a chemical compound with the molecular formula C10H9NO3. It is a derivative of oxazolidinone, a heterocyclic compound containing an oxazole ring fused to a lactam ring. The 3-benzoyl group in 2-Oxazolidinone,3-benzoyl-5-methyl- is an acyl group derived from benzoic acid, which is attached to the oxazolidinone ring, while the 5-methyl group is a methyl substituent attached to the same ring. 2-Oxazolidinone,3-benzoyl-5-methyl- is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various organic compounds. It is characterized by its unique structure and reactivity, which can be further explored for its properties and potential uses in chemical research and development.

7007-16-1

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7007-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7007-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7007-16:
(6*7)+(5*0)+(4*0)+(3*7)+(2*1)+(1*6)=71
71 % 10 = 1
So 7007-16-1 is a valid CAS Registry Number.

7007-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzoyl-5-methyl-1,3-oxazolidin-2-one

1.2 Other means of identification

Product number -
Other names 3-benzoyl-5-methyl-oxazolidin-2-one

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:7007-16-1 SDS

7007-16-1Downstream Products

7007-16-1Relevant academic research and scientific papers

Synthesis of Chiral Selenazolines from N-Acyloxazolidinones via a Selenative Rearrangement of Chiral Cyclic Skeletons

Shibahara, Fumitoshi,Fukunaga, Tomoki,Kubota, Saki,Yoshida, Akihito,Murai, Toshiaki

supporting information, p. 5826 - 5830 (2018/09/25)

A synthetic route to chiral selenazolines from readily available N-acyloxazolidinones via a selenative rearrangement of a chiral cyclic skeleton is reported. The reaction proceeds in the presence of elemental selenium, a hydrochlorosilane, and an amine. A

Decarboxylative isomerization of N-Acyl-2-oxazolidinones to 2-oxazolines

May, Aaron E.,Willoughby, Patrick H.,Hoye, Thomas R.

, p. 3292 - 3294 (2008/09/20)

(Chemical Equation Presented) N-Acyl-2-oxazolidinones are ring-opened by lithium iodide and decarboxylated in the presence of a mild proton source. Further reaction with an amine base provides 2-oxazolines. The transformation is general for oxazolidinones unsubstituted in the 5 position and occurs under mild conditions (25-50°C). These results complement the existing methods for this transformation by allowing lower temperatures and/or avoiding metal catalysts.

A facile one-pot solid-phase synthesis of oxazolidin-2-ones using polymer-supported 2-hydroxyalkyl selenide reagent

Hu, Qiao-Sheng,Sheng, Shou-Ri,Lin, Shu-Ying,Wei, Mei-Hong,Xin, Qin,Liu, Xiao-Ling

, p. 74 - 75 (2008/02/04)

A simple, efficient and environmentally friendly procedure for one-pot solid-phase synthesis of 2-oxazolidinones in moderate to good yields by reaction of polystyrene-supported 2-hydroxyalkyl selenide with benzoyl isocyanate and subsequent oxidation/cycli

Cycloaddition Reaction of Heterocumulenes with Oxiranes Catalyzed by an Organotin Iodide-Lewis Base Complex

Shibata, Ikuya,Baba, Akio,Iwasaki, Hiroyuki,Matsuda, Haruo

, p. 2177 - 2184 (2007/10/02)

Organotin halide-Lewis base complexes are versatile catalysts for the cycloaddition of heterocumulenes with oxiranes and afford good yields of five-membered heterocyclic compounds under mild and neutral conditions.The catalysts are sufficiently active tha

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