Cas 99212-06-3,(1'S, 5R, 6R)-5-isopropenyl-2-methyl-6-(1'-methyl-2'-nitroethyl)-cyclohex-2-en-1-one

99212-06-3

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Basic information

Product Name: (1'S, 5R, 6R)-5-isopropenyl-2-methyl-6-(1'-methyl-2'-nitroethyl)-cyclohex-2-en-1-one
Synonyms: (1'S, 5R, 6R)-5-isopropenyl-2-methyl-6-(1'-methyl-2'-nitroethyl)-cyclohex-2-en-1-one
CAS NO:99212-06-3
Molecular Formula:
Molecular Weight: 237.299
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'S, 5R, 6R)-5-isopropenyl-2-methyl-6-(1'-methyl-2'-nitroethyl)-cyclohex-2-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (1'S, 5R, 6R)-5-isopropenyl-2-methyl-6-(1'-methyl-2'-nitroethyl)-cyclohex-2-en-1-one(99212-06-3)
EPA Substance Registry System: (1'S, 5R, 6R)-5-isopropenyl-2-methyl-6-(1'-methyl-2'-nitroethyl)-cyclohex-2-en-1-one(99212-06-3)

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: 99212-06-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 99212-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,1 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99212-06:
(7*9)+(6*9)+(5*2)+(4*1)+(3*2)+(2*0)+(1*6)=143
143 % 10 = 3
So 99212-06-3 is a valid CAS Registry Number.

99212-06-3Upstream product

99212-06-3Downstream Products

99212-06-3Relevant academic research and scientific papers

Nitro-olefin bicycloannulation: one-step synthesis of tricyclo2,7>octan-6-ones from cyclohexenones and of tricyclo2,6>heptan-3-ones from cyclopentenones

Cory, Robert M.,Anderson, Paul C.,Bailey, Murray D.,McLaren, Fred R.,Renneboog, Richard M.,Yamamoto, Brian R.

, p. 2618 - 2627 (2007/10/02)

Nitro-olefins bicycloannulate the α'-enolates of α-cyclohexenones and α-cyclopentenones by initial addition at -78 deg C, followed by further reaction in situ in the presence of hexamethylphosphoramide in refluxing tetrahydrofuran to give tricyclo3.2.1.0

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