Cas 1088435-28-2,1-(2-hydroxy-1-phenylethyl)-4-isopropenyl-hexahydro-cyclopenta[b]pyrrol-2-one

1088435-28-2

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Basic information

Product Name: 1-(2-hydroxy-1-phenylethyl)-4-isopropenyl-hexahydro-cyclopenta[b]pyrrol-2-one
Synonyms: 1-(2-hydroxy-1-phenylethyl)-4-isopropenyl-hexahydro-cyclopenta[b]pyrrol-2-one
CAS NO:1088435-28-2
Molecular Formula:
Molecular Weight: 285.386
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: 1-(2-hydroxy-1-phenylethyl)-4-isopropenyl-hexahydro-cyclopenta[b]pyrrol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-hydroxy-1-phenylethyl)-4-isopropenyl-hexahydro-cyclopenta[b]pyrrol-2-one(1088435-28-2)
EPA Substance Registry System: 1-(2-hydroxy-1-phenylethyl)-4-isopropenyl-hexahydro-cyclopenta[b]pyrrol-2-one(1088435-28-2)

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: 1088435-28-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1088435-28-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,8,4,3 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1088435-28:
(9*1)+(8*0)+(7*8)+(6*8)+(5*4)+(4*3)+(3*5)+(2*2)+(1*8)=172
172 % 10 = 2
So 1088435-28-2 is a valid CAS Registry Number.

1088435-28-2Upstream product

1088435-27-1 6-isopropenyl-3-phenyl-2,3,5,5a,6,7-hexahydro-1-oxa-3a-azacyclopenta[c]pentalen-4(8H)-one

1088435-28-2Downstream Products

1088435-28-2Relevant academic research and scientific papers

Intramolecular ene reaction of a chiral bicyclic lactam

Resek, James E.

experimental part, p. 9792 - 9794 (2009/04/07)

(Chemical Equation Presented) The preparation of bicylic lactam 2 is described, employing an acetoacetate-based synthesis of 1,4-ketoacid 3. The lactam 2 was shown to undergo a thermal ene reaction at 280-300°C to afford tricycle 7. Reduction of the ene product followed by removal of the chiral auxiliary fragment provided the unusual lactam system 9 in highly enantioenriched form.

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