Cas 112389-01-2,1-(m-chloroanilino)-2,7-di(m-chlorophenyl)-2,7-diazatetracyclo<4.4.2.0<sup>3,12</sup>.0<sup>8,11</sup>>dodecane-4,10-dione

112389-01-2

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Basic information

Product Name: 1-(m-chloroanilino)-2,7-di(m-chlorophenyl)-2,7-diazatetracyclo<4.4.2.0^3,12.0^8,11>dodecane-4,10-dione
Synonyms:
CAS NO:112389-01-2
Molecular Formula:
Molecular Weight: 538.861
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: 1-(m-chloroanilino)-2,7-di(m-chlorophenyl)-2,7-diazatetracyclo<4.4.2.0^3,12.0^8,11>dodecane-4,10-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-(m-chloroanilino)-2,7-di(m-chlorophenyl)-2,7-diazatetracyclo<4.4.2.0^3,12.0^8,11>dodecane-4,10-dione(112389-01-2)
EPA Substance Registry System: 1-(m-chloroanilino)-2,7-di(m-chlorophenyl)-2,7-diazatetracyclo<4.4.2.0^3,12.0^8,11>dodecane-4,10-dione(112389-01-2)

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: 112389-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112389-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112389-01:
(8*1)+(7*1)+(6*2)+(5*3)+(4*8)+(3*9)+(2*0)+(1*1)=102
102 % 10 = 2
So 112389-01-2 is a valid CAS Registry Number.

112389-01-2Upstream product

71581-98-1 2,4-di-m-chloroanilinocyclopent-2-enone

112389-01-2Downstream Products

112389-01-2Relevant academic research and scientific papers

Rearrangements in the Furan Series. III. Reactions of 2,4-Diarylaminocyclopent-2-enones with Nucleophiles

D'Arcy, Bruce R.,Lewis, Keith G.,Mulquiney, Colin E.

, p. 509 - 521 (2007/10/02)

Alcoholysis of the 4-arylamino group of a number of 2,4-diarylaminocyclopent-2-enones occurs readily to form the 4-alkoxy derivatives.Under suitable conditions a number of other nucleophiles yielded a variety of 4-substituted 2-arylaminocyclopent-2-enones.As by-products of these reactions several compounds having a novel tetracyclic structure were isolated.

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