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Trimethyl 2,5-diphenyl-N-(1',2'-dimethoxycarbonylethenyl)-3-pyrroline-2,3,4-tricarboxylate is a complex organic compound with the molecular formula C26H25NO8. It is characterized by a pyrroline ring, which is a five-membered ring containing one nitrogen atom, and three carboxylate groups attached to the 2, 3, and 4 positions. The molecule also features two phenyl groups at the 2 and 5 positions, and a dimethoxycarbonylethenyl group attached to the nitrogen atom. trimethyl 2,5-diphenyl-N-(1',2'-dimethoxycarbonylethenyl)-3-pyrroline-2,3,4-tricarboxylate is a derivative of pyrroline, a heterocyclic compound with potential applications in the synthesis of various pharmaceuticals and other organic compounds. Its structure and properties make it an interesting target for chemical research and development.

89330-94-9

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89330-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89330-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,3 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89330-94:
(7*8)+(6*9)+(5*3)+(4*3)+(3*0)+(2*9)+(1*4)=159
159 % 10 = 9
So 89330-94-9 is a valid CAS Registry Number.

89330-94-9Downstream Products

89330-94-9Relevant academic research and scientific papers

X=Y-ZH compounds as potential 1,3-dipoles. Part 30. Cycloaddition of arylidene imines of α-amino esters to acetylenic dipolarophiles and pyrrole forming rearrangements

Grigg, Ronald,Gunaratne, H. Q. Nimal,Kemp, James

, p. 6467 - 6482 (2007/10/02)

Arylidene imines of α-amino esters undergo cycloaddition to ethyl phenylpropiolate, methyl propiolate and dimethyl acetylenedicarboxylate (ADE) on heating in toluene (110°C)or o-xylene (135- 145°C). The reactions proceed via stereospecific azomethine ylid

REACTION OF Δ3-PYRROLINES WITH DIMETHYL ACETYLENEDICARBOXYLATE. A NOVEL PYRROLE FORMING REARRANGEMENT

Grigg, Ronald,Gunaratne, H.Q. Nimal,Kemp, James

, p. 99 - 102 (2007/10/02)

Reaction of arylidene imines of methyl phenylglycinate with 2 moles of dimethyl acetylenedicarboxylate (ADE) leads, via an intermediate Δ3-pyrroline, to loss of the original methyl phenylglycinate moiety and formation of 2-aryl-3,4,5-tricarbo methoxypyrroles.

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