284491
(R)-(+)-2-Amino-3-phenyl-1-propanol
98%
Sinônimo(s):
D-Phenylalaninol
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About This Item
Fórmula linear:
C6H5CH2CH(NH2)CH2OH
Número CAS:
Peso molecular:
151.21
Beilstein:
2208239
Número CE:
Número MDL:
Código UNSPSC:
12352116
ID de substância PubChem:
NACRES:
NA.22
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Ensaio
98%
forma
solid
atividade óptica
[α]/D +22.8°, c = 1.2 in 1 M HCl
pf
93-95 °C (lit.)
grupo funcional
amine
hydroxyl
phenyl
cadeia de caracteres SMILES
N[C@@H](CO)Cc1ccccc1
InChI
1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m1/s1
chave InChI
STVVMTBJNDTZBF-SECBINFHSA-N
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Dam. 1 - Skin Corr. 1B
Código de classe de armazenamento
8A - Combustible corrosive hazardous materials
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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W W Mak et al.
Canadian journal of biochemistry, 58(12), 1421-1429 (1980-12-01)
The activities of a range of phenylalaninol-related compounds on capping of concanavalin A and induction of rounding of Chinese hamster ovary tsHl cells, as well as on the fluidity of phosphatidylcholine-cholesterol (1:1) liposomes, have been examined. These compounds include phenylalaninol
Gretta C M'bitsi-Ibouily et al.
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M O Blondel et al.
Biochemical and biophysical research communications, 150(3), 979-986 (1988-02-15)
The illumination of Escherichia coli cells with UVA light, 320 nm less than or equal to lambda less than or equal to 380 nm, triggers a transient growth and division delay. The built-in 4-thiouridine chromophore which absorbs light at 340
W W Mak et al.
Canadian journal of biochemistry, 58(9), 737-744 (1980-09-01)
This study describes a rounding reaction induced in mammalian cells by the addition of phenylalaninol. In the Chinese hamster ovary tsH1 line the rounding occurred rapidly with a half time of 1 min at 25 mM phenylalaninol. After the removal
Violetta Constantinou-Kokotou et al.
Journal of peptide science : an official publication of the European Peptide Society, 11(7), 431-435 (2005-01-07)
2-Oxoamides based on long chain beta-amino acids were synthesized. 1-Benzyl substituted long chain amines, needed for such synthesis, were synthesized starting from Boc-phenylalaninol. The oxidative conversion of a phenyl group to a carboxyl group was used as the key transformation
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