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Documentos Principais

279897

Sigma-Aldrich

(R)-(−)-2-Phenylpropionic acid

97%

Sinônimo(s):

(R)-(−)-Hydratropic acid, (R)-HTA

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About This Item

Fórmula linear:
CH3CH(C6H5)CO2H
Número CAS:
Peso molecular:
150.17
Beilstein:
2207688
Número MDL:
Código UNSPSC:
12352002
ID de substância PubChem:
NACRES:
NA.22

Ensaio

97%

Formulário

solid

atividade óptica

[α]20/D −72°, c = 1.6 in chloroform

pureza óptica

ee: 98% (HPLC)

índice de refração

n20/D 1.523 (lit.)

p.e.

115 °C/1 mmHg (lit.)

pf

29-30 °C (lit.)

densidade

1.1 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

C[C@@H](C(O)=O)c1ccccc1

InChI

1S/C9H10O2/c1-7(9(10)11)8-5-3-2-4-6-8/h2-7H,1H3,(H,10,11)/t7-/m1/s1

chave InChI

YPGCWEMNNLXISK-SSDOTTSWSA-N

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Aplicação

Chiral building block. Resolving agent

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - 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)

230.0 °F - closed cup

Ponto de fulgor (°C)

110 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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D Ahmad et al.
Chirality, 6(5), 365-371 (1994-01-01)
The significance of disturbances of lipid metabolism caused by xenobiotic acyl-CoAs as possible causes of peroxisomal proliferation has been studied with the enantiomers of 2-phenylpropionic acid (2-PPA), the (R)-enantiomer of which is converted to the acyl-CoA in rats while its
A J Hutt et al.
Chirality, 5(8), 596-601 (1993-01-01)
The metabolism of (R,S)-ibuprofen has been investigated in 24 microbial cultures. Of these Cunninghamella elegans, Mucor hiemalis, and Verticillium lecanii catalyzed the oxidation of the drug to 2-[4-(2-hydroxy-2-methylpropyl)phenyl]propionic acid, a known mammalian metabolite. The extent of metabolism was greatest with
D K Bhattacharyya et al.
The Journal of biological chemistry, 271(4), 2179-2184 (1996-01-26)
Examination of the crystal structure of the ovine prostaglandin endoperoxide synthase-1 (PGHS-1)/S- flurbiprofen complex (Picot, D., Loll, P.J., and Garavito, R.M. (1994) Nature 367, 243-2491) suggests (a) that the carboxyl group of arachidonic acid interacts with the arginino group of

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