Cas 75516-79-9,trimethyl c-5-(4-nitrophenyl)-2-phenylpyrrolodine-r-2,c-3,c-4-tricarboxylate

75516-79-9

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Basic information

Product Name: trimethyl c-5-(4-nitrophenyl)-2-phenylpyrrolodine-r-2,c-3,c-4-tricarboxylate
Synonyms:
CAS NO:75516-79-9
Molecular Formula:
Molecular Weight: 442.425
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: trimethyl c-5-(4-nitrophenyl)-2-phenylpyrrolodine-r-2,c-3,c-4-tricarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: trimethyl c-5-(4-nitrophenyl)-2-phenylpyrrolodine-r-2,c-3,c-4-tricarboxylate(75516-79-9)
EPA Substance Registry System: trimethyl c-5-(4-nitrophenyl)-2-phenylpyrrolodine-r-2,c-3,c-4-tricarboxylate(75516-79-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 75516-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75516-79-9 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, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75516-79:
(7*7)+(6*5)+(5*5)+(4*1)+(3*6)+(2*7)+(1*9)=149
149 % 10 = 9
So 75516-79-9 is a valid CAS Registry Number.

75516-79-9Upstream product

75516-79-9Downstream Products

75516-79-9Relevant 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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