Cas 412015-11-3,2-[(3,4-Dimethoxy-benzyl)-(2-ethoxycarbonyl-acetyl)-amino]-dec-9-enoic acid ethyl ester

412015-11-3

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Basic information

Product Name: 2-[(3,4-Dimethoxy-benzyl)-(2-ethoxycarbonyl-acetyl)-amino]-dec-9-enoic acid ethyl ester
Synonyms: 2-[(3,4-Dimethoxy-benzyl)-(2-ethoxycarbonyl-acetyl)-amino]-dec-9-enoic acid ethyl ester
CAS NO:412015-11-3
Molecular Formula:
Molecular Weight: 477.598
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-[(3,4-Dimethoxy-benzyl)-(2-ethoxycarbonyl-acetyl)-amino]-dec-9-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(3,4-Dimethoxy-benzyl)-(2-ethoxycarbonyl-acetyl)-amino]-dec-9-enoic acid ethyl ester(412015-11-3)
EPA Substance Registry System: 2-[(3,4-Dimethoxy-benzyl)-(2-ethoxycarbonyl-acetyl)-amino]-dec-9-enoic acid ethyl ester(412015-11-3)

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: 412015-11-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 412015-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,0,1 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 412015-11:
(8*4)+(7*1)+(6*2)+(5*0)+(4*1)+(3*5)+(2*1)+(1*1)=73
73 % 10 = 3
So 412015-11-3 is a valid CAS Registry Number.

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412015-11-3Relevant academic research and scientific papers

Syntheses of (-)-(7S)- and (+)-(7R)-K252a dimers

Tamaki, Kazuhiko,Huntsman, Elliott W.D,Petsch, Dejah T,Wood, John L

, p. 379 - 382 (2007/10/03)

This letter describes syntheses of (-)-(7S)-and (+)-(7R)-K252a dimers wherein a convergent bis-indole-N-glycosidic coupling step was used for the resolution of the C(7) substituted (±)-aglycon. Dimerization of the derived monomers was achieved via olefin methathesis.

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