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B5136

Sigma-Aldrich

Benzylamine hydrochloride

Sinônimo(s):

Phenylmethylamine

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About This Item

Fórmula linear:
C6H5CH2NH2·HCl
Número CAS:
3287-99-8
Peso molecular:
143.61
Número CE:
221-943-6
Número MDL:
MFCD00012852
Código UNSPSC:
12352100
ID de substância PubChem:
57653937
NACRES:
NA.22

forma

crystals

pf

262-263 °C (lit.)

cadeia de caracteres SMILES

Cl.NCc1ccccc1

InChI

1S/C7H9N.ClH/c8-6-7-4-2-1-3-5-7;/h1-5H,6,8H2;1H

chave InChI

XKXHCNPAFAXVRZ-UHFFFAOYSA-N

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Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H302,H315,H318,H335

Classificações de perigo

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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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Sigma-Aldrich

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Sigma-Aldrich

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1,3-Acetonedicarboxylic acid technical grade

Sigma-Aldrich

165115

1,3-Acetonedicarboxylic acid

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Glutamatergic N-methyl-D-aspartate (NMDA) receptors have critical roles in several neurological and psychiatric diseases. Dizocilpine (MK-801) is a ligand at phencyclidine recognition sites that is associated with NMDA receptor-coupled cation channels, where it acts as a potent noncompetitive antagonist of central
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ACS chemical neuroscience, 8(7), 1519-1529 (2017-03-24)
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A versatile synthesis of unsaturated seven-membered ring lactams has been developed. The sequence involves hydroamination of Baylis-Hillman acetate with amines, followed by intramolecular cyclocarbonylation reactions of the resulting allylamines. This process can tolerate a wide array of functional groups, and
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