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126993

Sigma-Aldrich

N-Ethylbenzylamine

97%

Sinónimos:

N-Benzylethylamine

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About This Item

Fórmula lineal:
C6H5CH2NHCH2CH3
Número de CAS:
14321-27-8
Peso molecular:
135.21
Beilstein/REAXYS Number:
386023
EC Number:
238-265-1
MDL number:
MFCD00009031
UNSPSC Code:
12352100
PubChem Substance ID:
24847753
NACRES:
NA.22

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.511 (lit.)

bp

191-194 °C (lit.)

density

0.909 g/mL at 25 °C (lit.)

functional group

amine
phenyl

SMILES string

CCNCc1ccccc1

InChI

1S/C9H13N/c1-2-10-8-9-6-4-3-5-7-9/h3-7,10H,2,8H2,1H3

InChI key

HVAAHUDGWQAAOJ-UHFFFAOYSA-N

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Application

N-Ethylbenzylamine has been used to demonstrate the reactivity of NDTE (2,5-dihydroxyphenylacetic acid, 2,5-bis-tetrahydropyranyl ether p-nitrophenyl ester) and HLTE (homogentisic gamma-lactone tetrahydropyranyl ether). It has also been used to prepare 2-[(N-Benzyl, N-ethyl)amino]derivative using 2-chloro-4H-pyrido[1,2-a]pyrimidin-4-one.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
MKCS8194
MKCQ5414
MKCH1409
MKCH1142
MKCD9105

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N-Benzylethylenediamine 97%

Sigma-Aldrich

462292

N-Benzylethylenediamine

M J Rose et al.
Analytical chemistry, 71(11), 2221-2230 (1999-06-15)
Two new reagents, NDTE (2,5-dihydroxyphenylacetic acid, 2,5-bis-tetrahydropyranyl ether p-nitrophenyl ester) and HLTE (homogentisic gamma-lactone tetrahydropyranyl ether), are described for the chemical derivatization of primary and/or secondary amines to form an electrochemically active product. These reagents undergo reaction with the aforementioned
M Di Braccio et al.
Il Farmaco; edizione scientifica, 43(9), 705-723 (1988-09-01)
The N,N-disubstituted 4-amino-2H-pyrido[1,2-a]pyrimidin-2-ones (III) and isomer 2-amino-4H-pyrido[1,2-a]pyrimidin-4-ones (IV) were obtained from the reaction of 2-aminopyridine with the N,N-disubstituted ethyl malonamate/phosphorus oxychloride reagent (II), in refluxing 1,2-dichloroethane. 2-[(N-Benzyl, N-ethyl)amino]derivative (IV b) was also prepared in excellent yield by treating 2-chloro-4H-pyrido[1,2-a]pyrimidin-4-one (V)
Md Salman Shakil et al.
Biomedicines, 9(2) (2021-01-31)
Hydroxypyr(id)ones are a pharmaceutically important class of compounds that have shown potential in diverse areas of drug discovery. We investigated the 3-hydroxy-4-pyridones 1a-1c and 3-hydroxy-4-thiopyridones 1d-1f as well as their Ru(η6-p-cymene)Cl complexes 2a-2f, and report here the molecular structures of
Oh Kyung Choi et al.
Journal of hazardous materials, 403, 123636-123636 (2020-08-28)
Solvent extraction desalination (SED) is one of the liquid-liquid separation techniques that selectively uptake freshwater from high saline water, and then separate the absorbed freshwater from the solvent through temperature swing. This study evaluated the desalination performance of seven different

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