Cas 898540-89-1,10-hydroxy-13-(4-methoxy-benzyl)-12-oxo-2-oxa-13-aza-bicyclo[14.2.2]eicosa-1<sup>(19)</sup>,4,10,16<sup>(20)</sup>,17-pentaene-14-carboxylic acid methyl ester

898540-89-1

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Basic information

Product Name: 10-hydroxy-13-(4-methoxy-benzyl)-12-oxo-2-oxa-13-aza-bicyclo[14.2.2]eicosa-1⁽¹⁹⁾,4,10,16⁽²⁰⁾,17-pentaene-14-carboxylic acid methyl ester
Synonyms: 10-hydroxy-13-(4-methoxy-benzyl)-12-oxo-2-oxa-13-aza-bicyclo[14.2.2]eicosa-1⁽¹⁹⁾,4,10,16⁽²⁰⁾,17-pentaene-14-carboxylic acid methyl ester
CAS NO:898540-89-1
Molecular Formula:
Molecular Weight: 479.573
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: 10-hydroxy-13-(4-methoxy-benzyl)-12-oxo-2-oxa-13-aza-bicyclo[14.2.2]eicosa-1⁽¹⁹⁾,4,10,16⁽²⁰⁾,17-pentaene-14-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 10-hydroxy-13-(4-methoxy-benzyl)-12-oxo-2-oxa-13-aza-bicyclo[14.2.2]eicosa-1⁽¹⁹⁾,4,10,16⁽²⁰⁾,17-pentaene-14-carboxylic acid methyl ester(898540-89-1)
EPA Substance Registry System: 10-hydroxy-13-(4-methoxy-benzyl)-12-oxo-2-oxa-13-aza-bicyclo[14.2.2]eicosa-1⁽¹⁹⁾,4,10,16⁽²⁰⁾,17-pentaene-14-carboxylic acid methyl ester(898540-89-1)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 898540-89-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 898540-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,5,4 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 898540-89:
(8*8)+(7*9)+(6*8)+(5*5)+(4*4)+(3*0)+(2*8)+(1*9)=241
241 % 10 = 1
So 898540-89-1 is a valid CAS Registry Number.

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898540-89-1Relevant academic research and scientific papers

Synthetic studies toward macrocidins: an RCM approach for the construction of the central cyclic core

Ramana,Mondal, Mohabul A.,Puranik, Vedavati G.,Gurjar, Mukund K.

, p. 4061 - 4064 (2007/10/03)

The central macrocyclic core of the macrocidins was constructed using RCM as the key reaction. A preliminary investigation dealing with the key reactions, that is, the Dieckmann cyclization and the RCM, revealed that RCM of the β-ketoamide is better than

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