261742
N-Benzyl-2-phenethylamine
99%
Sinônimo(s):
N-Benzyl-2-phenylethylamine
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About This Item
Fórmula linear:
C6H5CH2CH2NHCH2C6H5
Número CAS:
Peso molecular:
211.30
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
Produtos recomendados
Ensaio
99%
índice de refração
n20/D 1.566 (lit.)
p.e.
327-328 °C/750 mmHg (lit.)
densidade
1.007 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
C(Cc1ccccc1)NCc2ccccc2
InChI
1S/C15H17N/c1-3-7-14(8-4-1)11-12-16-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2
chave InChI
UPABQMWFWCMOFV-UHFFFAOYSA-N
Aplicação
N-Benzyl-2-phenethylamine has been used in synthesis of dithiocarbamates.
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
235.4 °F - closed cup
Ponto de fulgor (°C)
113 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Elton Luiz Silva et al.
Journal of nanoscience and nanotechnology, 16(2), 1291-1300 (2016-07-20)
All-trans retinoic acid, a hydrophobic drug, has become one of the most successful examples of differentiation agents used for treatment of acute promyelocytic leukemia. On the other hand, histone deacetylase inhibitors, such as cholesteryl butyrate, present differentiating activity and.can potentiate
N Segovia et al.
Journal of applied toxicology : JAT, 22(6), 353-357 (2002-11-09)
Dithiocarbamates (DTCs) are chemicals featuring a great chelating capacity. The toxicological study of DTCs is very important in view of their relatively simple synthesis and wide array of sanitary and industrial applications. In this study, the toxicity of some of
Zsanett Dorkó et al.
Molecules (Basel, Switzerland), 23(6) (2018-05-31)
One of the main reasons for making molecularly imprinted polymers (MIPs) has been that MIPs interact selectively with a specific target compound. This claim is investigated here with the example of a widely used type of noncovalent MIP, the MIP
Valquíria T Arantes et al.
Colloids and surfaces. B, Biointerfaces, 188, 110749-110749 (2020-01-14)
Repair of tissue damaged in diabetic wounds is essential to minimize the cases of amputation of the limbs in millions of diabetic people around the world. Although the all-trans retinoic acid (ATRA) is described as a potential wound healing agent
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