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4-butyl-1,3-oxazolidine-2,5-dione is a chemical compound with the molecular formula C7H11NO3. It is a heterocyclic compound, specifically an oxazolidine derivative, which features a five-membered ring containing two oxygen atoms and one nitrogen atom. The compound is characterized by the presence of a butyl group (a four-carbon alkyl chain) attached to the nitrogen atom in the oxazolidine ring. This chemical is known for its potential applications in various industries, such as pharmaceuticals and materials science, due to its unique structure and properties. It is important to note that the specific uses, safety, and environmental impact of 4-butyl-1,3-oxazolidine-2,5-dione should be carefully considered and researched, as they can vary depending on the context and application.

6271-01-8

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6271-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6271-01-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6271-01:
(6*6)+(5*2)+(4*7)+(3*1)+(2*0)+(1*1)=78
78 % 10 = 8
So 6271-01-8 is a valid CAS Registry Number.

6271-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-butyl-1,3-oxazolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names -

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:6271-01-8 SDS

6271-01-8Downstream Products

6271-01-8Relevant academic research and scientific papers

Large-scale synthesis of α-amino acid-N-carboxyanhydrides

Semple, J. Edward,Sullivan, Bradford,Sill, Kevin N.

, p. 53 - 61 (2016/12/30)

Hetero- and homopolymers prepared from α-amino acid-N-carboxyanhydrides (NCAs) monomers are widely useful products. The preparation of pure NCA monomers has been extensively studied in the past. Purification methods including repeated crystallizations, extraction, and flash column chromatography have been devised. However, these methods are not easily amendable to large-scale NCA preparations. This article describes the synthesis of numerous highly purified NCAs on a >100 g scale using a simple filtration step through diatomaceous earth (celite). The resulting NCAs provided polyethylene glycol (PEG)–amino acid triblock polymers devoid of low-molecular-weight by-products that were routinely observed when unfiltered batches of NCAs were used. Also disclosed is the preparation of NCAs at ambient temperature. Traditionally, NCA reactions using a phosgene source are heated. This study shows these reactions can be driven by the slight exotherm that forms upon reagent mixing. This eliminates the need for an external heating source, simplifying large-scale reactions.

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