Catalog No.:AA0032F4

712-76-5 | 4-Phenylbenzylamine

Name: Name:4-Phenylbenzylamine
Brand: AABLOCKS
SKU: AA0032F4
Availability: InStock
Rating: 90 (10 reviews)

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Purity

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250mg

98%

in stock

$8.00 $6.00

- +

98%

in stock

$12.00 $8.00

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98%

in stock

$51.00 $36.00

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25g

95%

in stock

$197.00 $138.00

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100g

95%

in stock

$750.00 $525.00

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0032F4

Chemical Name:

4-Phenylbenzylamine

CAS Number:

712-76-5

Molecular Formula:

C13H13N

Molecular Weight:

183.2490

MDL Number:

MFCD01310838

SMILES:

NCc1ccc(cc1)c1ccccc1

NSC Number:

402180

Properties

BP:

325.1 °C at 760 mmHg

Form:

Solid

MP:

48-53°C(lit.);

Storage:

2-8℃;

Computed Properties

Complexity:

153

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

3.1

Downstream Synthesis Route

712-76-5

622-78-6

164470-64-8

76-05-1

4-(N'-benzyl-N''-biphenyl-4-ylmethyl-guanidinomethyl)-benzamide;compoundwithtrifluoro-aceticacid

[1]TetrahedronLetters,1999,vol.40,p.4477-4480

52395-66-1

712-76-5

164470-64-8

76-05-1

4-(N'-biphenyl-4-ylmethyl-N''-cyclohexylmethyl-guanidinomethyl)-benzamide;compoundwithtrifluoro-aceticacid

[1]TetrahedronLetters,1999,vol.40,p.4477-4480

712-76-5

164470-64-8

76-05-1

isothiocyanatomethyl-cyclopentane

4-(N'-biphenyl-4-ylmethyl-N''-cyclopentylmethyl-guanidinomethyl)-benzamide;compoundwithtrifluoro-aceticacid

[1]TetrahedronLetters,1999,vol.40,p.4477-4480

712-76-5

350716-60-8

350717-42-9

[1]Luo;Williams;Read;Curran[JournalofOrganicChemistry,2001,vol.66,#12,p.4261-4266]

3218-36-8

712-76-5

[1]Beller,Matthias;Chandrashekhar,VishwasG.;Jagadeesh,RajenahallyV.;Jiao,Haijun;Murugesan,Kathiravan;Wei,Zhihong[ChemicalScience,2020,vol.11,#17,p.4332-4339]

[2]Jagadeesh,RajenahallyV.;Murugesan,Kathiravan;Alshammari,AhmadS.;Neumann,Helfried;Pohl,Marga-Martina;Radnik,Jörg;Beller,Matthias[Science,2017,vol.358,#6361,p.326-332]

[3]Beller,Matthias;Chandrashekhar,VishwasG.;Gawande,ManojB.;Jagadeesh,RajenahallyV.;Kalevaru,NarayanaV.;Kamer,PaulC.J.;Senthamarai,Thirusangumurugan;Zbořil,Radek[ChemicalScience,2020,vol.11,#11,p.2973-2981]

[4]Boyd,HelenF.;Fell,StephenC.M.;Hickey,DeirdreM.B.;Ife,RobertJ.;Leach,ColinA.;Macphee,ColinH.;Milliner,KevinJ.;Pinto,IvanL.;Rawlings;Smith,StephenA.;Stansfield,IanG.;Stanway,StevenJ.;Theobald,ColinJ.;Whittaker,CarolineM.[BioorganicandMedicinalChemistryLetters,2002,vol.12,#1,p.51-55]

[5]Yraola,Francesc;García-Vicente,Silvia;Fernández-Recio,Juan;Albericio,Fernando;Zorzano,Antonio;Marti,Luc;Royo,Miriam[JournalofMedicinalChemistry,2006,vol.49,#21,p.6197-6208]

[6]Pedras,M.SoledadeC.;Sarma-Mamillapalle,VijayK.[JournalofAgriculturalandFoodChemistry,2012,vol.60,#32,p.7792-7798]

[7]Staroń,Jakub;Warszycki,Dawid;Kurczab,Rafał;Satała,Grzegorz;Bugno,Ryszard;Hogendorf,Adam;Bojarski,AndrzejJ.[RSCAdvances,2016,vol.6,#60,p.54918-54925]

[8]CurrentPatentAssignee:KOREAINSTITUTEOFSCIENCEANDTECHNOLOGY;HANYANGUNIVERSITY-KR101725292,2017,B1

Literature

Title: New efficient substrates for semicarbazide-sensitive amine oxidase/VAP-1 enzyme: analysis by SARs and computational docking.

Journal: Journal of medicinal chemistry 20061019

Title: A new series of glycopeptide antibiotics incorporating a squaric acid moiety. Synthesis, structural and antibacterial studies.

Journal: The Journal of antibiotics 20060901

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