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Tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-1,3-dione is a heterocyclic organic compound characterized by a pyrrolo-oxazole ring system. tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-1,3-dione consists of a pyrrolidine ring fused to an oxazole ring, with both nitrogen atoms in the respective rings contributing to the overall structure. The compound is a dione, indicating the presence of two carbonyl groups (C=O) within the molecule. It is an important intermediate in the synthesis of various biologically active compounds, such as alkaloids and pharmaceuticals, due to its unique structure and reactivity. The compound's properties, such as solubility and stability, can be influenced by the presence of substituents on the ring system, making it a versatile building block in organic synthesis.

5626-64-2

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5626-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5626-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5626-64:
(6*5)+(5*6)+(4*2)+(3*6)+(2*6)+(1*4)=102
102 % 10 = 2
So 5626-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO3/c8-5-4-2-1-3-7(4)6(9)10-5/h4H,1-3H2

5626-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7,7a-tetrahydropyrrolo[1,2-c][1,3]oxazole-1,3-dione

1.2 Other means of identification

Product number -
Other names EINECS 227-066-5

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:5626-64-2 SDS

5626-64-2Relevant academic research and scientific papers

Efficient preparation of proline N-carboxyanhydride using polymer-supported bases

Gulin, Oscar P.,Rabanal, Francesc,Giralt, Ernest

, p. 5385 - 5388 (2007/10/03)

A procedure for the preparation of proline N-carboxyanhydride in high yield and purity is described using polymer-supported tertiary amines. The polymer-supported amine can be recycled with a basic wash and filtration of the resin. The procedure facilitates the access to the efficient preparation of the polyproline polymer with potential therapeutic interest.

ENANTIOMERIC QUANTIFICATIONS OF AMINO ACIDS THROUGH THEIR Nα-ACYL AMIDES BY GAS CHROMATOGRAPHY.

Hosten, N.,Antenuis, M.J.O

, p. 48 - 50 (2007/10/02)

Apparent separation of 1.1 or higher on Chirasil Val III can be obtained for Nα-acyl N-alkyl aminoacid amides allowing the use of short capillary gas chromatographic columns.A clean derivatization protocol without racemization is described, proceding through the NCA derivatives that are prepared from "in situ" silylated amino acids with trimethylsilyl cyanide.

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