Cas 375385-88-9,<i>N</i>-[4-methoxy-2-(1-methyl-2-oxo-ethyl)-3-(2-oxo-ethyl)-phenyl]-benzamide

375385-88-9

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Basic information

Product Name: N-[4-methoxy-2-(1-methyl-2-oxo-ethyl)-3-(2-oxo-ethyl)-phenyl]-benzamide
Synonyms: N-[4-methoxy-2-(1-methyl-2-oxo-ethyl)-3-(2-oxo-ethyl)-phenyl]-benzamide
CAS NO:375385-88-9
Molecular Formula:
Molecular Weight: 325.364
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: N-[4-methoxy-2-(1-methyl-2-oxo-ethyl)-3-(2-oxo-ethyl)-phenyl]-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-methoxy-2-(1-methyl-2-oxo-ethyl)-3-(2-oxo-ethyl)-phenyl]-benzamide(375385-88-9)
EPA Substance Registry System: N-[4-methoxy-2-(1-methyl-2-oxo-ethyl)-3-(2-oxo-ethyl)-phenyl]-benzamide(375385-88-9)

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: 375385-88-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 375385-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,5,3,8 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 375385-88:
(8*3)+(7*7)+(6*5)+(5*3)+(4*8)+(3*5)+(2*8)+(1*8)=189
189 % 10 = 9
So 375385-88-9 is a valid CAS Registry Number.

375385-88-9Upstream product

174182-76-4 N-(4-methoxy-8-methyl-5,8-dihydronaphthalen-1-yl)benzamide

375385-88-9Downstream Products

375385-88-9Relevant academic research and scientific papers

The Diels-Alder reactions of quinone imine ketals: A versatile synthesis of highly substituted 5-methoxyindoles

Banfield, Scott C.,England, Dylan B.,Kerr, Michael A.

, p. 3325 - 3327 (2001)

Equation presented 32-71% overall N-Benzoylated quinone imine ketals undergo smooth cycloadditions in a [4 + 2] sense to yield the expected cycloadducts. The crude cycloadducts, when subjected to a short series of simple transformations, produce synthetic

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