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5(4H)-Oxazolone, 2-(phenylmethyl)-, also known as 2-benzyl-5(4H)-oxazolone, is an organic compound with the molecular formula C10H9NO2. It is a heterocyclic compound containing an oxazolone ring, which is a five-membered ring with two oxygen atoms and one nitrogen atom. The phenylmethyl group (benzyl) is attached to the 2-position of the oxazolone ring, providing a phenyl ring connected to a methyl group. 5(4H)-Oxazolone, 2-(phenylmethyl)- is often used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. It can be synthesized through various methods, such as the condensation of α-amino acids with aldehydes or ketones, and is known for its stability and versatility in chemical reactions.

1078-60-0

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1078-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1078-60-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1078-60:
(6*1)+(5*0)+(4*7)+(3*8)+(2*6)+(1*0)=70
70 % 10 = 0
So 1078-60-0 is a valid CAS Registry Number.

1078-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-4H-1,3-oxazol-5-one

1.2 Other means of identification

Product number -
Other names 2-Benzyl-oxazolin-5-on

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:1078-60-0 SDS

1078-60-0Relevant academic research and scientific papers

An efficient synthesis of aryl phenaceturates using acid catalyzed dicyclohexylcarbodiimide esterification and transient N-tert-butoxycarbonylation

Cabaret,Liu,Wakselman

, p. 480 - 482 (2007/10/02)

Application of the Holmberg procedure (DCC/pyridine/p-TSA(cat)) improves the yield of the direct condensation of phenols with phenylacetylglycine (1). Moreover, N-tert-butoxycarbonylation of 1 impedes an intramolecular reaction leading to an oxazolone, an

CONTRASTING THERMAL BEHAVIOUR OF DIASTEREOISOMERIC 4-ACETYLTHIO-3-ACYLAMINO-1-(α-TRIPHENYLPHOSPHORANYLIDENE)ALKOXYCARBONYLMETHYLAZETIDIN-2-ONES

Irving, James R.,Perrone, Ettore,Stoodley, Richard J.

, p. 2501 - 2504 (2007/10/02)

Under conditions in which cis isomers of the title compounds are converted into 6β-acylamino-2-methylpenem-3-carboxylates, trans isomers afford thiazole-4-carboxylates and 2-alkyloxazolin-5-ones.

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