Cas 869115-88-8,(5S,8S)-8-[N-(benzyloxycarbonyl)amino]-6-azabicyclo[10.4.0]hexadeca-1<sup>(12)</sup>,13,15-triene-2,10-diyne-5-carboxylic acid N-methyl amide

869115-88-8

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Basic information

Product Name: (5S,8S)-8-[N-(benzyloxycarbonyl)amino]-6-azabicyclo[10.4.0]hexadeca-1⁽¹²⁾,13,15-triene-2,10-diyne-5-carboxylic acid N-methyl amide
Synonyms: (5S,8S)-8-[N-(benzyloxycarbonyl)amino]-6-azabicyclo[10.4.0]hexadeca-1⁽¹²⁾,13,15-triene-2,10-diyne-5-carboxylic acid N-methyl amide
CAS NO:869115-88-8
Molecular Formula:
Molecular Weight: 429.475
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: (5S,8S)-8-[N-(benzyloxycarbonyl)amino]-6-azabicyclo[10.4.0]hexadeca-1⁽¹²⁾,13,15-triene-2,10-diyne-5-carboxylic acid N-methyl amide(CAS DataBase Reference)
NIST Chemistry Reference: (5S,8S)-8-[N-(benzyloxycarbonyl)amino]-6-azabicyclo[10.4.0]hexadeca-1⁽¹²⁾,13,15-triene-2,10-diyne-5-carboxylic acid N-methyl amide(869115-88-8)
EPA Substance Registry System: (5S,8S)-8-[N-(benzyloxycarbonyl)amino]-6-azabicyclo[10.4.0]hexadeca-1⁽¹²⁾,13,15-triene-2,10-diyne-5-carboxylic acid N-methyl amide(869115-88-8)

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: 869115-88-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 869115-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,1,1 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 869115-88:
(8*8)+(7*6)+(6*9)+(5*1)+(4*1)+(3*5)+(2*8)+(1*8)=208
208 % 10 = 8
So 869115-88-8 is a valid CAS Registry Number.

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869115-88-8Relevant academic research and scientific papers

The synthesis and evaluation of 10- and 12-membered ring benzofused enediyne amino acids

Du, Yanming,Creighton, Christopher J.,Yan, Zhengyin,Gauthier, Diane A.,Dahl, John P.,Zhao, Boyu,Belkowski, Stanley M.,Reitz, Allen B.

, p. 5936 - 5948 (2007/10/03)

The enediyne moiety is a versatile functional group found in natural anticancer and anti-infective agents, undergoing the Bergman cyclization reaction to afford a diradical which cleaves double-stranded DNA. We have incorporated the enediyne group into 10

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