Cas 1006594-49-5,ethyl 2,4-dihydroxy-3-methylene-6-(4-nitrophenyl)cyclohex-1-ene-1-carboxylate

1006594-49-5

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Basic information

Product Name: ethyl 2,4-dihydroxy-3-methylene-6-(4-nitrophenyl)cyclohex-1-ene-1-carboxylate
Synonyms: ethyl 2,4-dihydroxy-3-methylene-6-(4-nitrophenyl)cyclohex-1-ene-1-carboxylate
CAS NO:1006594-49-5
Molecular Formula:
Molecular Weight: 319.314
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: ethyl 2,4-dihydroxy-3-methylene-6-(4-nitrophenyl)cyclohex-1-ene-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2,4-dihydroxy-3-methylene-6-(4-nitrophenyl)cyclohex-1-ene-1-carboxylate(1006594-49-5)
EPA Substance Registry System: ethyl 2,4-dihydroxy-3-methylene-6-(4-nitrophenyl)cyclohex-1-ene-1-carboxylate(1006594-49-5)

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: 1006594-49-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1006594-49-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,5,9 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1006594-49:
(9*1)+(8*0)+(7*0)+(6*6)+(5*5)+(4*9)+(3*4)+(2*4)+(1*9)=135
135 % 10 = 5
So 1006594-49-5 is a valid CAS Registry Number.

1006594-49-5Upstream product

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1006594-49-5Relevant academic research and scientific papers

An unexpected organocatalytic asymmetric tandem Michael/Morita-Baylis- Hillman reaction

Cabrera, Silvia,Aleman, Jose,Bolze, Patrick,Bertelsen, Soren,Jorgensen, Karl Anker

, p. 121 - 125 (2008/09/20)

(Chemical Equation Presented) Simply complex: An organocatalytic tandem Michael/Morita-Baylis-Hillman reaction has been developed in which secondary amine catalysts allow for a very selective, scalable synthesis of highly substituted optically active cycl

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