Cas 113397-20-9,(1R,6R)-1,6-Bis-(2-chloro-phenyl)-1,6-diphenyl-hexa-2,4-diyne-1,6-diol; compound with 2-methoxy-cyclohepta-2,4,6-trienone

113397-20-9

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Basic information

Product Name: (1R,6R)-1,6-Bis-(2-chloro-phenyl)-1,6-diphenyl-hexa-2,4-diyne-1,6-diol; compound with 2-methoxy-cyclohepta-2,4,6-trienone
Synonyms:
CAS NO:113397-20-9
Molecular Formula:
Molecular Weight: 619.544
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,6R)-1,6-Bis-(2-chloro-phenyl)-1,6-diphenyl-hexa-2,4-diyne-1,6-diol; compound with 2-methoxy-cyclohepta-2,4,6-trienone(CAS DataBase Reference)
NIST Chemistry Reference: (1R,6R)-1,6-Bis-(2-chloro-phenyl)-1,6-diphenyl-hexa-2,4-diyne-1,6-diol; compound with 2-methoxy-cyclohepta-2,4,6-trienone(113397-20-9)
EPA Substance Registry System: (1R,6R)-1,6-Bis-(2-chloro-phenyl)-1,6-diphenyl-hexa-2,4-diyne-1,6-diol; compound with 2-methoxy-cyclohepta-2,4,6-trienone(113397-20-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 113397-20-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113397-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113397-20:
(8*1)+(7*1)+(6*3)+(5*3)+(4*9)+(3*7)+(2*2)+(1*0)=109
109 % 10 = 9
So 113397-20-9 is a valid CAS Registry Number.

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113397-20-9Relevant academic research and scientific papers

HIGHLY SELECTIVE PHOTOREACTIONS OF α-OXOAMIDES AND α-TROPOLONE ALKYL ETHERS IN CRYSTALLINE INCLUSION COMPLEXES

Toda, Fumio,Tanaka, Koichi,Yagi, Minoru

, p. 1495 - 1502 (2007/10/02)

Control of photocyclization of three α-oxoamides in crystalline inclusion complexes with three kinds of host compounds was studied.In all cases, β-lactams were obtained exclusively.In two cases, cis-β-lactams were formed selectively.By an enantioselective

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