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2-[(5,5-dimethyl-3-oxocyclohex-1-enyl)amino]-3,6-dimethyl-benzonitrile hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146341-49-3

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146341-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146341-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 146341-49:
(8*1)+(7*4)+(6*6)+(5*3)+(4*4)+(3*1)+(2*4)+(1*9)=123
123 % 10 = 3
So 146341-49-3 is a valid CAS Registry Number.

146341-49-3Downstream Products

146341-49-3Relevant academic research and scientific papers

9-aminoacridine derivatives possessing psychotropic, antiamnestic and lipid-regulative activity

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, (2008/06/13)

"Derivatives of 9-aminoacridine characterized by psychothropic, antiamnestic and lipid-regulating activities". New chemical compounds derived of 9-aminoacridine with a general formula are presented: STR1 where R=H or CH3 R1 =H, CHsu

DERIVATIVES OF 9-AMINOACRIDINE HAVING PSYCHOTROPIC, ANTIAMNESTIC AND LIPID REGULATING PROPERTIES

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, (2008/06/13)

New chemical compounds, derivatives of 9-aminoacridine of general formula (I) where R = H, CH3; R1 = H, CH3, Br; R2 = H, CH3; R3 = alkyl-C1-C5, arylmethyl, diethylaminoethyl; X = C = O, CHOH; Y = CH2; X + Y = CH = CH; and their salts with organic and non-organic acids. The desired compounds are obtained by interaction of substituted nitriles of antranyl acid with dimedone with subsequent cyclization of intermediate enaminonitriles into corresponding ketones of 9-aminoacridine after the reduction of which and of their derivatives alkylated or aralkylated on the 9-amino group, the corresponding alcohols are obtained, after hydration of which 9-amino-3,4-dihydroacridines are obtained. When experimented on animals, the said derivatives of 9-aminoacridine have shown psychotropic, antiamnestic and lipid regulating properties, as well as a lower toxicity in comparison with known preparations.

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