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M31104

Sigma-Aldrich

α-Methylbenzylamine

99%

Sinônimo(s):

(±)-α-Methylbenzylamine, alpha-Methylbenzylamine, (±)-1-Phenylethylamine

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About This Item

Fórmula linear:
C6H5CH(CH3)NH2
Número CAS:
618-36-0
Peso molecular:
121.18
Beilstein:
636127
Número CE:
210-545-8
Número MDL:
MFCD00008069
Código UNSPSC:
12352100
ID de substância PubChem:
24896793
NACRES:
NA.22

Ensaio

99%

forma

liquid

índice de refração

n20/D 1.526 (lit.)

pb

185 °C/756 mmHg (lit.)

densidade

0.94 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CC(N)c1ccccc1

InChI

1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3

chave InChI

RQEUFEKYXDPUSK-UHFFFAOYSA-N

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Descrição geral

α-Methylbenzylamine is a nitrogen source that is widely used as a representative substrate to study the chemo-enzymatic kinetic resolution of primary amines.

Aplicação

α-Methylbenzylamine can be used as a reactant for the synthesis of dihydro-5H-dibenz[c,e]azepinium salts by reacting with racemic biphenol derivatives.
It is used in the synthesis of o-fluorobenzylamines.

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H302 + H312,H314

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

158.0 °F - closed cup

Ponto de fulgor (°C)

70 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Supelco

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Sigma-Aldrich

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Scientific reports, 7(1), 4786-4786 (2017-07-08)
The energy flow during natural photosynthesis is controlled by maintaining the spatial arrangement of pigments, employing helices as scaffolds. In this study, we have developed porphyrin-peptoid (pigment-helix) conjugates (PPCs) that can modulate the donor-acceptor energy transfer efficiency with exceptional precision
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Whole-cell biocatalysis based on metabolically active baker's yeast with engineered transamination activity can be used to generate molecules carrying a chiral amine moiety. A prerequisite is though to express efficient ω-transaminases and to reach sufficient intracellular precursor levels. Herein, the
Palladium-Catalyzed ortho-Selective C-H Fluorination of Oxalyl Amide-Protected Benzylamines.
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