Cas 85657-50-7,2-(4-Benzyloxy-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid methyl ester

85657-50-7

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Basic information

Product Name: 2-(4-Benzyloxy-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid methyl ester
Synonyms:
CAS NO:85657-50-7
Molecular Formula:
Molecular Weight: 470.481
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: 2-(4-Benzyloxy-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-Benzyloxy-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid methyl ester(85657-50-7)
EPA Substance Registry System: 2-(4-Benzyloxy-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid methyl ester(85657-50-7)

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: 85657-50-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85657-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,5 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85657-50:
(7*8)+(6*5)+(5*6)+(4*5)+(3*7)+(2*5)+(1*0)=167
167 % 10 = 7
So 85657-50-7 is a valid CAS Registry Number.

85657-50-7Upstream product

78246-50-1 (R)-(4-Benzyloxy-phenyl)-[(R)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-propionylamino]-acetic acid methyl ester

85657-50-7Downstream Products

85657-50-7Relevant academic research and scientific papers

IMPROVED ASYMMETRIC SYNTHESIS OF (-)-3-AMINOCARDICINIC ACID AND FURTHER OBSERVATIONS OF THE MITSUNOBU REACTION FOR β-LACTAM FORMATION IN SERYL PEPTIDES

Townsend, Craig A.,Nguyen, Loan T.

, p. 4859 - 4862 (1982)

Protected seryl peptide 2 was treated under a variety of conditions with triphenylphosphine or triethylphosphine and diethyl azodicarboxylate to give mechanistic insight into the β-lactam forming reaction and an improved route to (-)-3-aminocardicinic aci

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