Cas 935261-50-0,2-[(S)-1-{5-[N-(methoxymethyl)-1H-indol-3-yl]oxazol-2-yl}-2-phenylethyl]isoindoline-1,3-dione

935261-50-0

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Basic information

Product Name: 2-[(S)-1-{5-[N-(methoxymethyl)-1H-indol-3-yl]oxazol-2-yl}-2-phenylethyl]isoindoline-1,3-dione
Synonyms: 2-[(S)-1-{5-[N-(methoxymethyl)-1H-indol-3-yl]oxazol-2-yl}-2-phenylethyl]isoindoline-1,3-dione
CAS NO:935261-50-0
Molecular Formula:
Molecular Weight: 477.519
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-[(S)-1-{5-[N-(methoxymethyl)-1H-indol-3-yl]oxazol-2-yl}-2-phenylethyl]isoindoline-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(S)-1-{5-[N-(methoxymethyl)-1H-indol-3-yl]oxazol-2-yl}-2-phenylethyl]isoindoline-1,3-dione(935261-50-0)
EPA Substance Registry System: 2-[(S)-1-{5-[N-(methoxymethyl)-1H-indol-3-yl]oxazol-2-yl}-2-phenylethyl]isoindoline-1,3-dione(935261-50-0)

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: 935261-50-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 935261-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,2,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 935261-50:
(8*9)+(7*3)+(6*5)+(5*2)+(4*6)+(3*1)+(2*5)+(1*0)=170
170 % 10 = 0
So 935261-50-0 is a valid CAS Registry Number.

935261-50-0Upstream product

935261-50-0Downstream Products

935261-51-1 (S)-1-{5-[N-(methoxymethyl)-1H-indol-3-yl]oxazol-2-yl}-2-phenylethanamine

935261-50-0Relevant academic research and scientific papers

Iminophosphorane-based preparation of 2,5-disubstituted oxazole derivatives: Synthesis of the marine alkaloid almazole C

Fresneda, Pilar M.,Casta?eda, Marta,Blug, Mathias,Molina, Pedro

, p. 324 - 326 (2007)

A four-steps synthesis (32% overall yield) of marine alkaloid almazole C isolated from the red seaweed Haraldiophylum sp. is described. The key step, construction of the central 2,5-disubstituted oxazole ring is based on the aza-Wittig reaction of the imi

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