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Trimethyl 2,t-5-diphenylpyrrolodine-r-2,t-3,t-4-tricarboxylate is a complex organic compound with the molecular formula C26H23NO6. It is characterized by a pyrrolodine core, which is a type of heterocyclic compound containing a nitrogen atom in a five-membered ring. The molecule features two phenyl groups attached to the pyrrolodine ring, contributing to its structural complexity. The term "trimethyl" indicates the presence of three methyl groups, which are simple alkyl groups consisting of one carbon atom bonded to three hydrogen atoms. The compound also has three carboxylate groups, which are negatively charged functional groups derived from carboxylic acids. These features collectively contribute to the compound's chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

75516-80-2

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75516-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75516-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,1 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75516-80:
(7*7)+(6*5)+(5*5)+(4*1)+(3*6)+(2*8)+(1*0)=142
142 % 10 = 2
So 75516-80-2 is a valid CAS Registry Number.

75516-80-2Downstream Products

75516-80-2Relevant academic research and scientific papers

Cycloaddition vs. Michael Addition in the Metal Halide/Amine-Induced Reactions of α-(Alkylideneamino) Esters with Electron-Deficient Olefins

Kanemasa, Shuji,Yoshioka, Manabu,Tsuge, Otohiko

, p. 869 - 874 (2007/10/02)

The lithiated intermediate derived from methyl 2-(benzylideneamino)propanoate and lithium bromide/triethylamine undergoes cycloaddition and Michael addition with methyl acrylate. 1,3-Dipole character of the intermediate is suggested on the basis of the pr

X=Y-ZH Systems as Potential 1,3-Dipoles. Part 7. Stereochemistry of the Cycloaddition of Imines of α-Amino Acid Esters to Fumarate and Maleate Esters

Grigg, Ronald,Kemp, James,Warnock, William J.

, p. 2275 - 2284 (2007/10/02)

Aryl imines of α-amino acid esters undergo 1,3-dipolar cycloadditions with maleate and fumarate esters in quantitative yield when heated in boiling toluene to give mixtures of mainly two pyrrolidines.The major isomer in each case arises from cycloaddition

X=Y-ZH SYSTEMS AS POTENTIAL 1,3-DIPOLES. THE STEREOCHEMISTRY AND REGIOCHEMISTRY OF CYCLOADDITION REACTIONS OF IMINES OF α-AMINO-ACID ESTERS.

Grigg, Ronald,Kemp, James

, p. 2461 - 2464 (2007/10/02)

The stereochemistry and regiochemistry of cycloadditions of α-amino acid ester imines is dependent both on imine structure and on the reactivity of the dipolarophile.Phenylglycine imines undergo competing dipole stereomutation and cycloaddition with some dipolarophiles.

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