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Methyl 4-[(Z)-{4-oxo-3-[4-oxo-4-(1,3-thiazol-2-ylamino)butyl]-2-thioxo-1,3-thiazolidin-5-ylidene}methyl]benzoate is a complex organic compound with the molecular formula C20H15N3O5S2. It is characterized by a benzoate group attached to a 1,3-thiazolidine ring, which in turn is connected to a butyl chain containing a 1,3-thiazole moiety. The compound exhibits a Z-configuration, indicating the geometric arrangement of its double bond. This chemical is known for its potential applications in pharmaceutical research, particularly in the development of new drugs, due to its unique structure and reactivity. However, it is important to note that the specific uses, safety, and effectiveness of methyl 4-[(Z)-{4-oxo-3-[4-oxo-4-(1,3-thiazol-2-ylamino)butyl]-2-thioxo-1,3-thiazolidin-5-ylidene}methyl]benzoate in practical applications would require further investigation and validation through scientific studies.

6069-89-2

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6069-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6069-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6069-89:
(6*6)+(5*0)+(4*6)+(3*9)+(2*8)+(1*9)=112
112 % 10 = 2
So 6069-89-2 is a valid CAS Registry Number.

6069-89-2SDS

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 methyl 4-[[4-oxo-3-[4-oxo-4-(1,3-thiazol-2-ylamino)butyl]-2-sulfanylidene-1,3-thiazolidin-5-ylidene]methyl]benzoate

1.2 Other means of identification

Product number -
Other names METHYL 4-[(Z)-[4-OXO-2-SULFANYLIDENE-3-[3-(1,3-THIAZOL-2-YLCARBAMOYL)PROPYL]THIAZOLIDIN-5-YLIDENE]METHYL]BENZOATE

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:6069-89-2 SDS

6069-89-2Downstream Products

6069-89-2Relevant academic research and scientific papers

Synthesis of Norbornanones with a Geminal Dimethyl Group

Buchbauer, Gerhard,Dworan, Erich

, p. 1165 - 1174 (2007/10/02)

The synthesis of gem-dimethylnorbornanones is described.One synthetic pathway after a Diels-Alder reaction involves the transformation of the nitro group into the oxo group with subsequent methylation into the geminal dimethyl product.A shorter way by -cycloaddition of cyclopentadiene with a suitable dimethylated dienophile (e.g. 2-methyl-1-nitropropene) failed, probably by steric hindrance of the dienophile. 7-Oxanorbornanones with a gem -dimethyl group could not be prepared.A second synthetic approach to gem-dimethylnorbornanones is opened by Lewis acid catalyzed rearrangement of cyclohexenylcarbaldehydes. - Keywords: Camphenilone; Diels-Alder reaction; Homonorbornanone; α-Methylation of carbonyls; Nef-reaction; Norepifenchone

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