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4-benzyl-6-(phenoxathiin-2-yl)-3-(N-phthalyl-DL-alanyl)oxy-pyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

667466-74-2

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667466-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 667466-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,7,4,6 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 667466-74:
(8*6)+(7*6)+(6*7)+(5*4)+(4*6)+(3*6)+(2*7)+(1*4)=212
212 % 10 = 2
So 667466-74-2 is a valid CAS Registry Number.

667466-74-2Downstream Products

667466-74-2Relevant academic research and scientific papers

γ-oxo carboxylic acids in heterocyclic synthesis IV. Synthesis of some pyridazines containing phthalyl and tosyl amino acids using DCC as the condensing agent

Aly,Wasfy

, p. 1911 - 1921 (2003)

The 3(2H)-oxo-, 3(2H)-thioxo- or 3-amino-pyridazine derivatives 4, 6 and 7 were coupled with N-phthalyl- or N-tosyl-amino acids in one-step using N,N′-dicyclohexyl-carbodiimide as the condensing agent to furnish the corresponding 3-(N-phthalyl- or N-tosyl-aminoacyl)pyridazine derivatives 8-10 respectively. Hydrazinolysis of the N-phthalyl derivatives in methanol yielded the corresponding unprotected derivatives 11-13. The antibacterial activities of the prepared compounds were tested.

γ-oxo carboxylic acids in heterocyclic synthesis: Part IV - Synthesis of some pyridazines containing phthalyl and tosyl amino acids using DCC as the condensing agent

Aly,Wasfy

, p. 629 - 635 (2007/10/03)

3(2H)-Oxo-, 3-mercapto- or 3-amino-pyridazine derivatives 3,5 and 6 have been coupled with N-phthalyl- or N-tosyl-amino acids in one-step at room temperature by using N,N′-dicyclohexylcarbodiimide as the condensing agent to furnish the corresponding 3-N-(phthalyl- or tosyl-amino acids) pyridazine derivatives (7-9)a-h, respectively. Hydrazinolysis of the N-phthalyl derivatives (7-9)a-d in methanol yields the corresponding unprotected derivatives (7-9)M 9)i-l. The anti-bacterial activity of the prepared compounds has been tested.

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