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

1111644-91-7

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Basic information

Product Name: (1R,2R,3S,4R)-diethyl-4-hydroxy-4-(2-hydroxypropan-2-yl)-2-phenylcyclopentane-1,3-dicarboxylate
Synonyms: (1R,2R,3S,4R)-diethyl-4-hydroxy-4-(2-hydroxypropan-2-yl)-2-phenylcyclopentane-1,3-dicarboxylate
CAS NO:1111644-91-7
Molecular Formula:
Molecular Weight: 364.439
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: (1R,2R,3S,4R)-diethyl-4-hydroxy-4-(2-hydroxypropan-2-yl)-2-phenylcyclopentane-1,3-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3S,4R)-diethyl-4-hydroxy-4-(2-hydroxypropan-2-yl)-2-phenylcyclopentane-1,3-dicarboxylate(1111644-91-7)
EPA Substance Registry System: (1R,2R,3S,4R)-diethyl-4-hydroxy-4-(2-hydroxypropan-2-yl)-2-phenylcyclopentane-1,3-dicarboxylate(1111644-91-7)

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: 1111644-91-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1111644-91-7 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, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1111644-91:
(9*1)+(8*1)+(7*1)+(6*1)+(5*6)+(4*4)+(3*4)+(2*9)+(1*1)=107
107 % 10 = 7
So 1111644-91-7 is a valid CAS Registry Number.

1111644-91-7Upstream product

1111644-91-7Downstream Products

1111644-92-8 (1R,2R,3S)-diethyl 4-oxo-2-phenylcyclopentane-1,3-dicarboxylate

1111644-91-7Relevant academic research and scientific papers

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

Kaeobamrung, Juthanat,Bode, Jeffrey W.

, p. 677 - 680 (2009)

(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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