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104776-74-1

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104776-74-1 Usage

General Description

ETHYL 5-(2-BROMOACETYL)ISOXAZOLE-3-CARBOXYLATE is a chemical compound with the molecular formula C9H9BrNO4. It is an ester derivative of isoxazole-3-carboxylic acid that contains an ethyl group, a bromoacetyl group, and a carboxylate group. ETHYL 5-(2-BROMOACETYL)ISOXAZOLE-3-CARBOXYLATE has potential applications in medicinal chemistry and pharmaceutical research due to its interesting structural features and potential biological activities. It may also be used as a building block in the synthesis of more complex organic molecules. However, its specific properties and potential uses would need to be further studied and evaluated through experimental research.

Check Digit Verification of cas no

The CAS Registry Mumber 104776-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,7 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104776-74:
(8*1)+(7*0)+(6*4)+(5*7)+(4*7)+(3*6)+(2*7)+(1*4)=131
131 % 10 = 1
So 104776-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrNO4/c1-2-13-8(12)5-3-7(14-10-5)6(11)4-9/h3H,2,4H2,1H3

104776-74-1SDS

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 Ethyl 5-(2-bromoacetyl)isoxazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-(2-bromoacetyl)-1,2-oxazole-3-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:104776-74-1 SDS

104776-74-1Relevant articles and documents

Discovery of substituted (2‐aminooxazol‐4‐yl)isoxazole‐3‐ carboxylic acids as inhibitors of bacterial serine acetyltransferase in the quest for novel potential antibacterial adjuvants

Magalh?es, Joana,Franko, Nina,Raboni, Samanta,Annunziato, Giannamaria,Tammela, P?ivi,Bruno, Agostino,Bettati, Stefano,Armao, Stefano,Spadini, Costanza,Cabassi, Clotilde Silvia,Mozzarelli, Andrea,Pieroni, Marco,Campanini, Barbara,Costantino, Gabriele

, p. 1 - 16 (2021/03/16)

Many bacteria and actinomycetales use L‐cysteine biosynthesis to increase their tolerance to antibacterial treatment and establish a long‐lasting infection. In turn, this might lead to the onset of antimicrobial resistance that currently represents one of

Synthesis and pharmacological characterization of new analogs of broxaterol

De Amici,Conti,Dallanoce,Kassi,Castellano,Stefancich,De Micheli

, p. 69 - 80 (2007/10/03)

A series of isoxazole derivatives structurally related to broxaterol 1 has been prepared and tested for their potency to β1 and β2 adrenergic receptors. At variance with broxaterol, none of the tested compounds displayed agonistic activity. The 3-isopropenyl derivative 5f is the most potent antagonist both in the trachea and atria preparations.

Synthesis of New Isoxazole Aminoalcohols

Chiarino, D.,Fantucci, M.,Sala, A.,Veneziani, C.

, p. 337 - 342 (2007/10/02)

The preparation of new 1-isoxazolyl-2-amino-1-ethanol derivatives is described starting from the corresponding 1-isoxazolylethanones.It is also reported the synthesis of 1-(5-isoxazolyloxy)-3-amino-2-propanol compounds starting from the corresponding 5-ha

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