Cas 1111644-77-9,(3aS,4R,5R,6aS)-ethyl-4-(4-bromophenyl)-6a-hydroxy-1,1-dimethyl-3-oxohexahydro-1H-cyclopenta[c]furan-5-carboxylate

1111644-77-9

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Basic information

Product Name: (3aS,4R,5R,6aS)-ethyl-4-(4-bromophenyl)-6a-hydroxy-1,1-dimethyl-3-oxohexahydro-1H-cyclopenta[c]furan-5-carboxylate
Synonyms:
CAS NO:1111644-77-9
Molecular Formula:
Molecular Weight: 397.266
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: (3aS,4R,5R,6aS)-ethyl-4-(4-bromophenyl)-6a-hydroxy-1,1-dimethyl-3-oxohexahydro-1H-cyclopenta[c]furan-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,5R,6aS)-ethyl-4-(4-bromophenyl)-6a-hydroxy-1,1-dimethyl-3-oxohexahydro-1H-cyclopenta[c]furan-5-carboxylate(1111644-77-9)
EPA Substance Registry System: (3aS,4R,5R,6aS)-ethyl-4-(4-bromophenyl)-6a-hydroxy-1,1-dimethyl-3-oxohexahydro-1H-cyclopenta[c]furan-5-carboxylate(1111644-77-9)

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: 1111644-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1111644-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,1,6,4 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1111644-77:
(9*1)+(8*1)+(7*1)+(6*1)+(5*6)+(4*4)+(3*4)+(2*7)+(1*7)=109
109 % 10 = 9
So 1111644-77-9 is a valid CAS Registry Number.

1111644-77-9Upstream product

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1111644-77-9Relevant academic research and scientific papers

Stereodivergency of triazolium and imidazolium-derived NHcs for catalytic, enantioselective cyclopentane synthesis

Kaeobamrung, Juthanat,Bode, Jeffrey W.

supporting information; scheme or table, p. 677 - 680 (2009/08/08)

(Chemical Equation Presented) Chiral triazolium- and imidazolium-derived N-heterocyclic carbene catalysts promote the direct annulation of α,β-unsaturated aldehydes and achiral α-hydroxy enones to afford cyclopentane-fused lactones with high enantioselect

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