Cas 116218-29-2,1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(4-phenoxyphenyl)-, dihydrochloride

116218-29-2

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Basic information

Product Name: 1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(4-phenoxyphenyl)-, dihydrochloride
Synonyms:
CAS NO:116218-29-2
Molecular Formula: C20H26N2O2.2ClH
Molecular Weight: 399.361
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-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(4-phenoxyphenyl)-, dihydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(4-phenoxyphenyl)-, dihydrochloride(116218-29-2)
EPA Substance Registry System: 1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(4-phenoxyphenyl)-, dihydrochloride(116218-29-2)

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: 116218-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116218-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,1 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116218-29:
(8*1)+(7*1)+(6*6)+(5*2)+(4*1)+(3*8)+(2*2)+(1*9)=102
102 % 10 = 2
So 116218-29-2 is a valid CAS Registry Number.

116218-29-2Upstream product

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116218-29-2Relevant academic research and scientific papers

Evaluation of acrylophenones and related bis-Mannich bases against murine P388 leukemia

Dimmock, Jonathan R.,Patil, Shirish A.,Leek, Donald M.,Warrington, Robert C.,Fang, Wei D.

, p. 545 - 552 (2007/10/02)

2-Dimethylaminomethyl-1-(4-methoxyphenyl)-prop-2-en-1-one hydrochloride (IIa) was shown to have potent activity against P388 cells in vitro, whereas in vivo examination of this derivative and related acrylophenone hydrochlorides revealed little activity a

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