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5828-95-5

Ethyl (2E)-5-(1,3-benzodioxol-5-yl)-2-[(5-bromo-2-methoxyphenyl)methylidene]-7-methyl-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 C23H18BrN3O6S. It is characterized by a 1,3-benzodioxole ring, a 5-bromo-2-methoxyphenyl group, and a 7-methyl-3-oxo-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine core. The compound features a 2E configuration, indicating the presence of a trans double bond between the 2-[(5-bromo-2-methoxyphenyl)methylidene] and 5-(1,3-benzodioxol-5-yl) groups. It is an ethyl ester derivative, with an ethyl group attached to the 6-carboxylate position. This chemical is known for its potential applications in pharmaceutical research, particularly in the development of new therapeutic agents.

5828-95-5

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  • ethyl (2E)-5-(1,3-benzodioxol-5-yl)-2-[(5-bromo-2-methoxyphenyl)methylidene]-7-methyl-3-oxo-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

    Cas No: 5828-95-5

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  • ethyl (2E)-5-(1,3-benzodioxol-5-yl)-2-[(5-bromo-2-methoxyphenyl)methylidene]-7-methyl-3-oxo-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

    Cas No: 5828-95-5

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5828-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5828-95-5 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 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5828-95:
(6*5)+(5*8)+(4*2)+(3*8)+(2*9)+(1*5)=125
125 % 10 = 5
So 5828-95-5 is a valid CAS Registry Number.

5828-95-5SDS

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 (2E)-5-(1,3-benzodioxol-5-yl)-2-[(5-bromo-2-methoxyphenyl)methylidene]-7-methyl-3-oxo-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

1.2 Other means of identification

Product number -
Other names Trifluormethylmalonsaeuremethylethylester

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

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More Details:5828-95-5 SDS

5828-95-5Downstream Products

5828-95-5Relevant articles and documents

Synthesis of difluoromethylenemalonic acid esters and their reactions with trialkyl phosphites

Knunyants,Utebaev,Rokhlin,Lur'e,Mysov

, p. 873 - 875 (1976)

1. The electrophillic cleavage of alkyl fluorides from the esters of α-trifluoromethyl-β,β-dialkoxy-acrylic acids leads to the formation of esters of difluoromethylenemalonic acid. 2. During the reaction between the dimethyl ester of difluoromethylenemalonic acid and trimethylphosphite, a stable adduct is formed, which when heated splits into methyl difluorophosphite and the dimethyl ester of dimethoxymethylenemalonic acid.

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