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1,3,5-Triazabicyclo[3.2.0]hept-6-ene-2,4-dione,3-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

373367-46-5

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373367-46-5 Usage

Bicyclic compound

Yes
The molecule has two interconnected rings.

Heterocycle

Yes
The compound contains atoms other than carbon in its ring structure, specifically nitrogen and oxygen.

Nitrogen atoms

3

Carbonyl group

Yes
The compound contains a carbonyl group (C=O), which is a key functional group in organic chemistry.

Methyl group substitution

3-methyl
A methyl group (CH3) is added at the third position of the molecule, giving it the 3-methyl-(9CI) designation.

Derivative

1,3,5-Triazabicyclo[3.2.0]hept-6-ene-2,4-dione
The compound is derived from the parent compound 1,3,5-triazabicyclo[3.2.0]hept-6-ene-2,4-dione.

Potential applications

Organic synthesis, medicinal chemistry, material science
The compound may have uses in these fields, but further research and testing are required to confirm its specific applications and properties.

Further research needed

Yes
More investigation is necessary to determine the compound's specific uses, properties, and potential benefits in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 373367-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,3,3,6 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 373367-46:
(8*3)+(7*7)+(6*3)+(5*3)+(4*6)+(3*7)+(2*4)+(1*6)=165
165 % 10 = 5
So 373367-46-5 is a valid CAS Registry Number.

373367-46-5Downstream Products

373367-46-5Relevant academic research and scientific papers

Synthesis of Δ1-1,2-diazetines via a Diels-Alder cycloaddition approach

Breton, Gary W.,Shugart, John H.,Hughey, Christine A.,Perala, Suzanne M.,Hicks, Alisa D.

, p. 3185 - 3187 (2001)

(figure presented) A novel method for the synthesis of Δ1-1,2-diazetines is presented. Diels-Alder cycloaddition of dienophile 4 with five dienes afforded cycloadducts in good to excellent yields. Four of the obtained cycloadducts were converte

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