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2-Propenamide, 2-cyano-3-(dimethylamino)-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87164-96-3

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87164-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87164-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87164-96:
(7*8)+(6*7)+(5*1)+(4*6)+(3*4)+(2*9)+(1*6)=163
163 % 10 = 3
So 87164-96-3 is a valid CAS Registry Number.

87164-96-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-α-cyano-β-dimethylaminoacrylamide

1.2 Other means of identification

Product number -
Other names 2-cyano-3-(dimethylamino)-N-phenylacrylamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87164-96-3 SDS

87164-96-3Downstream Products

87164-96-3Relevant academic research and scientific papers

Synthesis, cytotoxic characterization, and SAR study of imidazo[1,2-b]pyrazole-7-carboxamides

Demjén, András,Alf?ldi, Róbert,Angyal, Anikó,Gyuris, Márió,Hackler, László,Szebeni, Gábor J.,W?lfling, János,Puskás, László G.,Kanizsai, Iván

, (2018/07/13)

The synthesis and in vitro cytotoxic characteristics of new imidazo[1,2-b]pyrazole-7-carboxamides were investigated. Following a hit-to-lead optimization exploiting 2D and 3D cultures of MCF-7 human breast, 4T1 mammary gland, and HL-60 human promyelocytic leukemia cancer cell lines, a 67-membered library was constructed and the structure–activity relationship (SAR) was determined. Seven synthesized analogues exhibited sub-micromolar activities, from which compound 63 exerted the most significant potency with a remarkable HL-60 sensitivity (IC50 = 0.183 μM).

α-Dimethylaminomethylenation-induced Houben-Hoesch-type cyclization of cyanoacetanilides: A practical synthesis of 3-formyl-4-hydroxyquinolin-2(1H)- ones

Kobayashi, Yusuke,Nakatani, Terue,Tanaka, Rie,Okada, Mari,Torii, Eri,Harayama, Takashi,Kimachi, Tetsutaro

experimental part, p. 3457 - 3463 (2011/06/17)

The tandem reaction of cyanoacetanilides with triflic anhydride in DMF proceeded at room temperature to afford 3-formyl-4-hydroxyquinolin-2(1H)-ones in good to high yields. A detailed mechanistic study revealed that the tandem reaction proceeded via α-dim

Reactions of diethyl 2-(ethoxymethylene)malonate with 2-cyanoacetanilides: Unexpected transfer of the ethoxymethylene moiety

Tkachova, Valeriya P.,Gorobets, Nikolay Yu.,Tkachov, Roman P.,Dyachenko, Oleksandr D.,Rusanov, Eduard B.,Dyachenko, Vladimir D.

scheme or table, p. 254 - 264 (2011/02/27)

A sodium ethoxide catalyzed reaction of N-substituted cyanoacetanilides 1a-f with diethyl 2-(ethoxymethylene)malonate 2 unexpectedly leads to the corresponding 2-amino-5-cyano-6-oxo-N,1-diaryl-1,6-dihydropyridine-3- carboxamides 3a-f, while the expected 5

ACETALS OF LACTAMS AND AMIDES. 42. REACTIONS OF ENAMINO AMIDES AND ENAMINO ESTERS WITH SOME FORMYLATING AGENTS. SYNTHESIS OF DERIVATIVES OF 2-PYRIDONE AND OF PYRIMIDIN-4- AND -6-ONES

Granik, V. G.,Ershov, L. V.,Grizik, S. I.,Chistyakov, V. V.

, p. 1026 - 1031 (2007/10/02)

The reactions of enamino esters and enamino amides with the diethyl acetal of dimethylformamide and with orthoformic ester have been investigated and it has been shown that the process takes place in two directions - with the formation of pyrimidone or 2-

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