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10-formyl-1,2,3,4-tetrahydropyrimido<1,2-a>indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100441-01-8

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100441-01-8 Usage

Type of compound

Heterocyclic compound

Structure

Contains a tetrahydropyrimidine ring fused with an indole ring

Functional group

Formyl group at the 10th position

Potential applications

Intermediate in the synthesis of pharmaceuticals and biologically active compounds

Importance

Important building block for medicinal chemistry

Unique features

Unique structure and reactivity

Research interest

Interesting target for chemical research and potential pharmaceutical applications

Chemical properties

May exhibit reactivity due to the presence of the formyl group and the fused heterocyclic rings

Physical properties

The specific physical properties (e.g., melting point, boiling point, solubility) are not provided in the material, but they can be determined experimentally or through computational methods.

Check Digit Verification of cas no

The CAS Registry Mumber 100441-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100441-01:
(8*1)+(7*0)+(6*0)+(5*4)+(4*4)+(3*1)+(2*0)+(1*1)=48
48 % 10 = 8
So 100441-01-8 is a valid CAS Registry Number.

100441-01-8Downstream Products

100441-01-8Relevant academic research and scientific papers

Synthesis of tricyclic-2-aminoindoles by intramolecular 1,3-dipolar cycloaddition of 1-ω-azidoalkylindoles

De la Mora, Marco A.,Cuevas, Erick,Muchowski, Joseph M.,Cruz-Almanza, Raymundo

, p. 5351 - 5353 (2001)

Thermolysis of the 1-ω-azidoalkylindoles 4, bearing an electron attracting substituent at C-3 (CHO, COMe, COOMe, CN) provides imidazo[1,2-a]indoles (5, n = 1), pyrimidino[1,2-a]indoles (5, n = 2), and 1,3-diazepino[1,2-a]indoles (5, n = 3).

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