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Benzenebutanamine, also known as β-phenyl-benzenebutanamine, is an organic compound with the chemical formula C10H13N. It is a derivative of benzenebutanamine, featuring a phenyl group (C6H5) attached to the β-carbon atom of the butanamine chain. Benzenebutanamine, b-phenyl- is a chiral molecule, meaning it has a non-superimposable mirror image, and can exist in two enantiomeric forms. Benzenebutanamine is a precursor in the synthesis of various pharmaceuticals and has potential applications in the development of drugs targeting the central nervous system. Its structure and properties make it an interesting subject for research in medicinal chemistry and drug design.

4444-70-6

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4444-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4444-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4444-70:
(6*4)+(5*4)+(4*4)+(3*4)+(2*7)+(1*0)=86
86 % 10 = 6
So 4444-70-6 is a valid CAS Registry Number.

4444-70-6Downstream Products

4444-70-6Relevant academic research and scientific papers

DEMETHYLASE ENZYMES INHIBITORS

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Page/Page column 64, (2013/10/21)

A compound of formula (I) and its use as an inhibitor of one or more histone demethylase enzymes.

Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1

Zhang, Pengtao,Yang, Xinye,Zhang, Feiran,Gabelli, Sandra B.,Wang, Renxiao,Zhang, Yihua,Bhat, Shridhar,Chen, Xiaochun,Furlani, Manuel,Amzel, L. Mario,Liu, Jun O.,Ma, Dawei

, p. 2600 - 2617 (2013/06/27)

Cellular protein synthesis is initiated with methionine in eukaryotes with few exceptions. Methionine aminopeptidases (MetAPs) which catalyze the process of N-terminal methionine excision are essential for all organisms. In mammals, type 2 MetAP (MetAP2)

Diastereoselective functionalisation of benzoannulated bicyclic sultams: Application for the synthesis of cis-2,4-diarylpyrrolidines

Kelleher, Susan,Quesne, Pierre-Yves,Evans, Paul

supporting information; experimental part, (2010/04/22)

The cis-dibromination of unsaturated bicyclic bridgehead sultams 5a and 5b, and experiments designed to understand the cisstereochemical outcome of these reactions, are described. In the case of 5b, a novel solvent dependent carbocation rearrangement occu

Synthesis of enantioenriched 2-substituted 4-phenylbutylamines by hydrogenolysis of optically pure 6-alkoxy-5,6-dihydro-4H-1,2-oxazines

Buchholz, Monika,Hiller, Florian,Reissig, Hans-Ulrich

, p. 2838 - 2843 (2007/10/03)

Lewis acid promoted exchange of the 6-ethoxy group of 6H- 1,2-oxazines 1-3 with (-)-menthol furnished the optically active heterocycles 4-6. Diastereomers 4a and 4b, which could be separated efficiently by chromatography, were excellent substrates for hig

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