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2-((4-(2-aminobenzylamino)butylamino)methyl)benzenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

287968-64-3

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287968-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287968-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,9,6 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 287968-64:
(8*2)+(7*8)+(6*7)+(5*9)+(4*6)+(3*8)+(2*6)+(1*4)=223
223 % 10 = 3
So 287968-64-3 is a valid CAS Registry Number.

287968-64-3Downstream Products

287968-64-3Relevant academic research and scientific papers

Synthesis and characterization of Bis-quinazolines from linear tetra-amines involving 2-(aminomethyl)benzenamine with aldehydes

Azadbakht, Reza,Khodabandeh, Maryame,Keypour, Hassan,Baghdad Abadi, Reza Haji Hosseini,Rudbari, Hadi Amiri

, p. 979 - 981 (2013)

Three tetra-amine compounds 2-((2-(2-aminobenzylamino)ethylamino)methyl) benzenamine (L1), 2-((3-(2-aminobenzylamino)propylamino)methyl) benzenamine (L2), and 2-((4-(2-aminobenzylamino)butylamino)methyl) benzenamine (L3) were synthesized and then their reaction with 2-hydroxybenzaldehyde, 2-nitrobenzaldehyde, and 2-hydroxy-3-methoxybenzaldehyde were investigated. Treatment of L1, L2, and L3 with the former aldehydes gave derivatives of quinazolines in a good yield. The products have been studied with IR, 1H NMR, 13C NMR, COSY, HMQC, and microanalysis.

Induction of apoptosis by aryl-substituted diamines: Role of aromatic group substituents and distance between nitrogens

Burns, Mark R,LaTurner, Solveig,Ziemer, Josh,McVean, Maralee,Devens, Bruce,Carlson,Graminski, Gerard F.,Vanderwerf, Scott M.,Weeks, Reitha S.,Carreon, Jay

, p. 1263 - 1267 (2007/10/03)

A series of aromatic substituted diamines was synthesized and characterized for their cytotoxic profiles against human breast and prostate tumor cell lines. Following a structure function analysis of the effects of changes of the benzyl substituents and t

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