Cas 1111644-47-3,(1S,2R,3R,5R)-ethyl-5-(2-hydroxypropan-2-yl)-7-oxo-2-phenyl-6-oxabicyclo[3.2.0]heptane-3-carboxylate

1111644-47-3

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Basic information

Product Name: (1S,2R,3R,5R)-ethyl-5-(2-hydroxypropan-2-yl)-7-oxo-2-phenyl-6-oxabicyclo[3.2.0]heptane-3-carboxylate
Synonyms: (1S,2R,3R,5R)-ethyl-5-(2-hydroxypropan-2-yl)-7-oxo-2-phenyl-6-oxabicyclo[3.2.0]heptane-3-carboxylate
CAS NO:1111644-47-3
Molecular Formula:
Molecular Weight: 318.37
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: (1S,2R,3R,5R)-ethyl-5-(2-hydroxypropan-2-yl)-7-oxo-2-phenyl-6-oxabicyclo[3.2.0]heptane-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,3R,5R)-ethyl-5-(2-hydroxypropan-2-yl)-7-oxo-2-phenyl-6-oxabicyclo[3.2.0]heptane-3-carboxylate(1111644-47-3)
EPA Substance Registry System: (1S,2R,3R,5R)-ethyl-5-(2-hydroxypropan-2-yl)-7-oxo-2-phenyl-6-oxabicyclo[3.2.0]heptane-3-carboxylate(1111644-47-3)

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: 1111644-47-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1111644-47-3 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, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1111644-47:
(9*1)+(8*1)+(7*1)+(6*1)+(5*6)+(4*4)+(3*4)+(2*4)+(1*7)=103
103 % 10 = 3
So 1111644-47-3 is a valid CAS Registry Number.

1111644-47-3Upstream product

1111644-47-3Downstream Products

1111644-91-7 (1R,2R,3S,4R)-diethyl-4-hydroxy-4-(2-hydroxypropan-2-yl)-2-phenylcyclopentane-1,3-dicarboxylate

1111644-47-3Relevant academic research and scientific papers

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

Kaeobamrung, Juthanat,Bode, Jeffrey W.

supporting information; experimental part, 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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