Cas 1314236-55-9,(1S,2R,3R)-ethyl 2-formyl-3-(furan-2-yl)-5-hydroxy-4'-methoxy-1,2,3,6-tetrahydro-[1,1'-biphenyl]-4-carboxylate

1314236-55-9

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Basic information

Product Name: (1S,2R,3R)-ethyl 2-formyl-3-(furan-2-yl)-5-hydroxy-4'-methoxy-1,2,3,6-tetrahydro-[1,1'-biphenyl]-4-carboxylate
Synonyms:
CAS NO:1314236-55-9
Molecular Formula:
Molecular Weight: 370.402
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)-ethyl 2-formyl-3-(furan-2-yl)-5-hydroxy-4'-methoxy-1,2,3,6-tetrahydro-[1,1'-biphenyl]-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,3R)-ethyl 2-formyl-3-(furan-2-yl)-5-hydroxy-4'-methoxy-1,2,3,6-tetrahydro-[1,1'-biphenyl]-4-carboxylate(1314236-55-9)
EPA Substance Registry System: (1S,2R,3R)-ethyl 2-formyl-3-(furan-2-yl)-5-hydroxy-4'-methoxy-1,2,3,6-tetrahydro-[1,1'-biphenyl]-4-carboxylate(1314236-55-9)

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: 1314236-55-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1314236-55-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,2,3 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1314236-55:
(9*1)+(8*3)+(7*1)+(6*4)+(5*2)+(4*3)+(3*6)+(2*5)+(1*5)=119
119 % 10 = 9
So 1314236-55-9 is a valid CAS Registry Number.

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1314236-55-9Relevant academic research and scientific papers

A general organocatalyzed Michael-Michael cascade reaction generates functionalized cyclohexenes

McGarraugh, Patrick G.,Jones, Joshua H.,Brenner-Moyer, Stacey E.

, p. 6309 - 6319 (2011/10/09)

Although β-dicarbonyl compounds are regularly employed as Michael donors, intermediates arising from the Michael addition of unsaturated β-ketoesters to α,β-unsaturated aldehydes are susceptible to multiple subsequent reaction pathways. We designed cyclic

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