Cas 116235-51-9,1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(2,4,5-trimethoxyphenyl) -, dihydrochloride

116235-51-9

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Basic information

Product Name: 1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(2,4,5-trimethoxyphenyl) -, dihydrochloride
Synonyms:
CAS NO:116235-51-9
Molecular Formula: C17H28N2O4.2ClH
Molecular Weight: 397.342
EINECS: N/A
Product Categories: N/A
Mol File: 116235-51-9.mol
Article Data: 1

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-(2,4,5-trimethoxyphenyl) -, dihydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(2,4,5-trimethoxyphenyl) -, dihydrochloride(116235-51-9)
EPA Substance Registry System: 1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(2,4,5-trimethoxyphenyl) -, dihydrochloride(116235-51-9)

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: 116235-51-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116235-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,3 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116235-51:
(8*1)+(7*1)+(6*6)+(5*2)+(4*3)+(3*5)+(2*5)+(1*1)=99
99 % 10 = 9
So 116235-51-9 is a valid CAS Registry Number.

116235-51-9Upstream product

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116235-51-9Relevant articles and documents

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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