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885954-76-7

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885954-76-7 Usage

General Description

Tert-butyl 4-oxoimidazolidine-1-carboxylate is a chemical compound with the molecular formula C9H15NO3. It is a derivative of imidazolidine-1-carboxylate, containing a tert-butyl group and a carbonyl group. tert-butyl 4-oxoimidazolidine-1-carboxylate is commonly used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It is known for its ability to undergo various chemical reactions, including esterification, amidation, and hydrolysis. Tert-butyl 4-oxoimidazolidine-1-carboxylate is considered to be a versatile building block in organic chemistry due to its reactivity and functional group compatibility.

Check Digit Verification of cas no

The CAS Registry Mumber 885954-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,9,5 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 885954-76:
(8*8)+(7*8)+(6*5)+(5*9)+(4*5)+(3*4)+(2*7)+(1*6)=247
247 % 10 = 7
So 885954-76-7 is a valid CAS Registry Number.

885954-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 4-oxoimidazolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 4-oxoimidazolidine-1-carboxylate

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:885954-76-7 SDS

885954-76-7Downstream Products

885954-76-7Relevant articles and documents

Synthesis of Enantioenriched gem-Disubstituted 4-Imidazolidinones by Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation

Sercel, Zachary P.,Sun, Alexander W.,Stoltz, Brian M.

, p. 6348 - 6351 (2021)

A variety of enantioenriched gem-disubstituted 4-imidazolidinones were prepared in up to >99% yield and 95% ee by the Pd-catalyzed decarboxylative asymmetric allylic alkylation of imidazolidinone-derived β-amidoesters. In the process of preparing these substrates, a rapid synthetic route to 4-imidazolidinone derivatives was developed, beginning from 2-thiohydantoin. The orthogonality of the benzoyl imide and tert-butyl carbamate groups used to protect these nitrogen-rich products was demonstrated, enabling potential applications in drug design.

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