Cas 121591-00-2,<3aR*-(1R*(or S*),2R*(or S*)3aα,4α,6aα)>-4-hydroxy-4-methyl-5-(4-morpholinyl)-3a-nitro-6-(2-nitro-cyclo-pentyl)-2,3,3a,4,5-hexahydropentalene

121591-00-2

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Basic information

Product Name: <3aR*-(1R*(or S*),2R*(or S*)3aα,4α,6aα)>-4-hydroxy-4-methyl-5-(4-morpholinyl)-3a-nitro-6-(2-nitro-cyclo-pentyl)-2,3,3a,4,5-hexahydropentalene
Synonyms:
CAS NO:121591-00-2
Molecular Formula:
Molecular Weight: 381.429
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: <3aR*-(1R*(or S*),2R*(or S*)3aα,4α,6aα)>-4-hydroxy-4-methyl-5-(4-morpholinyl)-3a-nitro-6-(2-nitro-cyclo-pentyl)-2,3,3a,4,5-hexahydropentalene(CAS DataBase Reference)
NIST Chemistry Reference: <3aR*-(1R*(or S*),2R*(or S*)3aα,4α,6aα)>-4-hydroxy-4-methyl-5-(4-morpholinyl)-3a-nitro-6-(2-nitro-cyclo-pentyl)-2,3,3a,4,5-hexahydropentalene(121591-00-2)
EPA Substance Registry System: <3aR*-(1R*(or S*),2R*(or S*)3aα,4α,6aα)>-4-hydroxy-4-methyl-5-(4-morpholinyl)-3a-nitro-6-(2-nitro-cyclo-pentyl)-2,3,3a,4,5-hexahydropentalene(121591-00-2)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 121591-00-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121591-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,5,9 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 121591-00:
(8*1)+(7*2)+(6*1)+(5*5)+(4*9)+(3*1)+(2*0)+(1*0)=92
92 % 10 = 2
So 121591-00-2 is a valid CAS Registry Number.

121591-00-2Upstream product

121591-00-2Downstream Products

121591-00-2Relevant academic research and scientific papers

CYCLOPENTAANNULATION REACTIONS BETWEEN NITROCYCLOALKENES AND DIACETYL MORPHOLINO ENAMINE

Felluga, F.,Nardin, G.,Nitti, P.,Pitacco, G.,Valentin, E.

, p. 6921 - 6928 (1988)

Hexahydro-pentalene and -indene nitroalcohols are obtained by reaction of 3-(4-morpholinyl)-3-buten-2-one with cyclic nitroolefins.With 1-nitro-cyclohexene a heterocyclization intermediate is separated, while an unusual product of double addition is obtained from the hexahydro-pentalene derivative in aqueous acidic medium.

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