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Trimethyl 2-benzyl-c-5-phenylpyrrolodine-r-2,c-3,c-4-tricarboxylate is a complex organic compound with the molecular formula C26H26N2O6. It is a derivative of pyrrolodine, a class of compounds known for their potential applications in pharmaceuticals and as chemical intermediates. This specific compound features a pyrrolodine core with a benzyl group at the 2-position and a phenyl group at the 5-position. The molecule also has three carboxyl groups attached to the pyrrolodine ring, which are esterified with trimethyl groups. These structural features contribute to its unique chemical properties and potential uses in various chemical and pharmaceutical applications.

75516-82-4

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75516-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75516-82-4 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 75516-82:
(7*7)+(6*5)+(5*5)+(4*1)+(3*6)+(2*8)+(1*2)=144
144 % 10 = 4
So 75516-82-4 is a valid CAS Registry Number.

75516-82-4Downstream Products

75516-82-4Relevant academic research and scientific papers

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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