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3-Ethyl-2H-1,3-benzoxazine-2,4(3H)-dione is a chemical compound with the molecular formula C10H9NO3. It is a derivative of benzoxazine, which is a heterocyclic compound consisting of a benzene ring fused to an oxazine ring. This specific compound features an ethyl group attached to the 3-position of the benzoxazine core, and it contains two carbonyl groups at the 2 and 4 positions, which are part of a 3H-dione structure. 3-ethyl-2H-1,3-benzoxazine-2,4(3H)-dione is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

2038-01-9

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2038-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2038-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2038-01:
(6*2)+(5*0)+(4*3)+(3*8)+(2*0)+(1*1)=49
49 % 10 = 9
So 2038-01-9 is a valid CAS Registry Number.

2038-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-1,3-benzoxazine-2,4-dione

1.2 Other means of identification

Product number -
Other names Benzo<1,3>oxazin-2,4-dione

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:2038-01-9 SDS

2038-01-9Downstream Products

2038-01-9Relevant academic research and scientific papers

The synthesis of cyclic and acyclic long-chain arylpiperazine derivatives of salicylamide as serotonin receptor ligands

Kowalski, Piotr,Jaskowska, Jolanta,Bojarski, Andrzej J.,Duszynska, Beata

, p. 209 - 214 (2008/09/18)

(Chemical Equation Presented) The 1-arylpiperazine series of N-substituted 1,3-benzoxazine-2,4-diones as well as O- and N-substituted salicylamides with an n-propyl chain were synthesized in order to explore the effect of cyclic and acyclic salicylamide moieties on their binding affinity for 5-HT1A, 5-HT2A and 5-HT7 receptor sites. Target compounds 1 and 2 were prepared by a two-step procedure, i.e. by alkylation of 1,3-benzoxazine-2,4-dione or salicylamide with 1,3-dibromopropane and next by condensation of 3-bromopropyl intermediates with arylpiperazines; syntheses of 3-bromopropyl intermediates were performed in solvent-free conditions. Compounds 3 were prepared by hydrolysis of 1. In respect of salicylamide moieties, binding affinities for 5-HT1A and 5-HT7 receptors increase according to the rank of derivatives 3 2A receptors, increased activity of ligands was changed in reverse order to the affinity for 5-HT1A, i.e. 2 1A and 5-HT7 receptor binding constants were the highest for the 2-methoxyphenyl ligand 2c, while the 3-chlorophenyl ligand 3b was most active for 5-HT2A receptors.

N-alkylation of imides using phase transfer catalysts under solvent-free conditions

Jaskowska, Jolanta,Kowalski, Piotr

experimental part, p. 1371 - 1375 (2009/04/07)

(Chemical Equation Presented) N-Alkylation of imides in the reaction of imides and alkylhalides, catalyzed by PT catalysts under solvent-free conditions, has been developed. The reaction occurs in the presence of K 2CO3, and in many cases it takes place spontaneously. In the N-benzylation reaction, it has been recognized that TBAB (tetrabutylammonium bromide) and TBATFB (tetrabutylammonium tetrafluoroborate) show highest catalytic effect. Versatility and synthetic capacity of the solvent-free alkylation has been confirmed by N-benzylation and N-ethylation of various imides. The developed procedure gives easy access to N-(ω-bromoalkyl) imides.

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