Cas 123250-86-2,(5S,12'E,14'E)-1-benzoyl-5-benzyl-3-(14-methylhexadeca-12',14'-dienyl)pyrrol-2(5H)-one

123250-86-2

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Basic information

Product Name: (5S,12'E,14'E)-1-benzoyl-5-benzyl-3-(14-methylhexadeca-12',14'-dienyl)pyrrol-2(5H)-one
Synonyms:
CAS NO:123250-86-2
Molecular Formula:
Molecular Weight: 511.748
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,12'E,14'E)-1-benzoyl-5-benzyl-3-(14-methylhexadeca-12',14'-dienyl)pyrrol-2(5H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (5S,12'E,14'E)-1-benzoyl-5-benzyl-3-(14-methylhexadeca-12',14'-dienyl)pyrrol-2(5H)-one(123250-86-2)
EPA Substance Registry System: (5S,12'E,14'E)-1-benzoyl-5-benzyl-3-(14-methylhexadeca-12',14'-dienyl)pyrrol-2(5H)-one(123250-86-2)

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: 123250-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123250-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,5 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123250-86:
(8*1)+(7*2)+(6*3)+(5*2)+(4*5)+(3*0)+(2*8)+(1*6)=92
92 % 10 = 2
So 123250-86-2 is a valid CAS Registry Number.

123250-86-2Upstream product

123250-87-3 (2E,4E)-16-Iodo-3-methyl-hexadeca-2,4-diene

123250-86-2Downstream Products

123250-86-2Relevant academic research and scientific papers

Cytochalasan Synthesis: Macrocycle Synthesis Using Intramolecular Diels-Alder Reactions. X-Ray Crystal Structure of 10-Phenylcytochalasa-6(7),13t-diene-1,21-dione

Harkin, Shaun A.,Jones, Richard H.,Tapolczay, David J.,Thomas, Eric J.

, p. 489 - 497 (2007/10/02)

An approach to the total synthesis of cytochalasans has been developed which makes use of an intramolecular Diels-Alder reaction to close the large ring simultaneously forming the hydrogenated isoindolone unit with the desired stereochemistry.Conjugated t

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