Cas 97911-65-4,(R)-(2-Hydroxy-3,5-dimethoxy-4-methyl-phenyl)-((1R,4R,7S,8S)-9-methyl-2-oxo-3,9-diaza-tricyclo[5.2.1.0<sup>4,8</sup>]dec-5-en-3-yl)-acetic acid methyl ester

97911-65-4

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Basic information

Product Name: (R)-(2-Hydroxy-3,5-dimethoxy-4-methyl-phenyl)-((1R,4R,7S,8S)-9-methyl-2-oxo-3,9-diaza-tricyclo[5.2.1.0^4,8]dec-5-en-3-yl)-acetic acid methyl ester
Synonyms:
CAS NO:97911-65-4
Molecular Formula:
Molecular Weight: 402.447
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: (R)-(2-Hydroxy-3,5-dimethoxy-4-methyl-phenyl)-((1R,4R,7S,8S)-9-methyl-2-oxo-3,9-diaza-tricyclo[5.2.1.0^4,8]dec-5-en-3-yl)-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-(2-Hydroxy-3,5-dimethoxy-4-methyl-phenyl)-((1R,4R,7S,8S)-9-methyl-2-oxo-3,9-diaza-tricyclo[5.2.1.0^4,8]dec-5-en-3-yl)-acetic acid methyl ester(97911-65-4)
EPA Substance Registry System: (R)-(2-Hydroxy-3,5-dimethoxy-4-methyl-phenyl)-((1R,4R,7S,8S)-9-methyl-2-oxo-3,9-diaza-tricyclo[5.2.1.0^4,8]dec-5-en-3-yl)-acetic acid methyl ester(97911-65-4)

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: 97911-65-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97911-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97911-65:
(7*9)+(6*7)+(5*9)+(4*1)+(3*1)+(2*6)+(1*5)=174
174 % 10 = 4
So 97911-65-4 is a valid CAS Registry Number.

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97911-65-4Relevant academic research and scientific papers

THE TOTAL SYNTHESIS OF (+/-)-NAPHTHYRIDINOMYCIN. II. CONSTRUCTION OF THE PENTACYCLIC CARBON SKELETON.

Evans, David A.,Biller, Scott A.

, p. 1911 - 1914 (2007/10/02)

A synthesis of an advanced pentacyclic intermediate to the quinone antibiotic naphthyridinomycin (1) is described.The stereoselective synthesis of 2b from tricyclic lactam 3 features a regio- and stereoselective, intermolecular amidoalkylation reaction and a Friedel-Crafts ring closure to annelate the aromatic nucleus.

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