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Ethyl (2Z)-2-[(5-bromo-2-hydroxy-3-nitrophenyl)methylidene]-7-methyl-5-[4-(methylsulfanyl)phenyl]-3-oxo-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate is a complex organic compound with a molecular formula of C22H18BrN3O5S2. It is characterized by a thiazolo[3,2-a]pyrimidine core, which is a heterocyclic ring system containing sulfur and nitrogen atoms. The molecule features a 5-bromo-2-hydroxy-3-nitrophenyl group attached to the methylene bridge, a methylsulfanylphenyl group, and a 7-methyl substituent. The compound also has a 3-oxo group and a carboxylate functional group, which is esterified with an ethyl group. This chemical is likely to be found in the realm of pharmaceuticals or as an intermediate in the synthesis of various biologically active molecules due to its intricate structure and potential for diverse interactions with biological targets.

5824-50-0

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5824-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5824-50-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5824-50:
(6*5)+(5*8)+(4*2)+(3*4)+(2*5)+(1*0)=100
100 % 10 = 0
So 5824-50-0 is a valid CAS Registry Number.

5824-50-0SDS

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 ethyl (2Z)-2-[(5-bromo-2-hydroxy-3-nitrophenyl)methylidene]-7-methyl-5-(4-methylsulfanylphenyl)-3-oxo-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

1.2 Other means of identification

Product number -
Other names Acetyl-aethyldisulfid

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:5824-50-0 SDS

5824-50-0Downstream Products

5824-50-0Relevant academic research and scientific papers

Unsymmetrical Organotrisulfide Formation via Low-Temperature Disulfanyl Anion Transfer to an Organothiosulfonate

Ali, Doaa,Hunter, Roger,De Doncker, Stephen,Rees-Jones, Sophie C. M.,Kaschula, Catherine H.

, p. 2862 - 2869 (2019/03/23)

New methodology is presented for the formation of unsymmetrical organotrisulfides in a high yield and purity, relatively free of polysulfide byproducts. The highlight of the method is the low-temperature (-78 °C) deprotection of a disulfanyl acetate with sodium methoxide in THF to form a disulfanyl anion, which reacts rapidly in situ with an organothiosulfonate (S-aryl or S-alkyl) within 30 seconds followed by quenching. The discovery of these new reaction conditions together with the relative greenness of the chemistry overall makes for an efficient protocol, from which a range of organotrisulfides covering aliphatic, aromatic, as well as cysteine and sugar groups can be accessed in a high yield and purity.

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