(S)-3-PHENYLBUTYRIC ACID

(S)-3-PHENYLBUTYRIC ACID Struktur
772-15-6
CAS-Nr.
772-15-6
Englisch Name:
(S)-3-PHENYLBUTYRIC ACID
Synonyma:
(S)-3-PHENYLBUTYRIC ACID;(S)-3-Phenylbutanoic acid;(3S)-3-Phenylbutyric acid;(3S)-3-Phenylbutanoic acid;(S)-3-Phenylisobutyric acid;(s)-β-methylhydrocinnamic acid;[S,(+)]-2-Benzylpropionic acid;(S)-BETA-METHYLHYDROCINNAMIC ACID;(S)-α-Methylbenzenepropionic acid;(2S)-2-Methyl-3-phenylpropanoic acid
CBNumber:
CB3664399
Summenformel:
C10H12O2
Molgewicht:
164.2
MOL-Datei:
772-15-6.mol

(S)-3-PHENYLBUTYRIC ACID Eigenschaften

Siedepunkt:
94-95 °C0.3 mm Hg(lit.)
Dichte
1.069 g/mL at 20 °C(lit.)
Brechungsindex
n20/D 1.518
pka
4.67±0.10(Predicted)

Sicherheit

S-Sätze: 23-24/25
WGK Germany  3

(S)-3-PHENYLBUTYRIC ACID Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:

S23:Gas/Rauch/Dampf/Aerosol nicht einatmen(geeignete Bezeichnung(en) vom Hersteller anzugeben).
S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

optical purity >99%

Verwenden

(S)-3-Phenylbutyric Acid is used as a sole carbon and energy source in the isolation of Rhodococcus rhodochrous PB1 from compost soil.Also, it is used in the design and synthesis of 2-Acylaminopyridin-4-ylimidazoles as p38 MAP kinase inhibitors in the treatment of many inflammatory disorders.

läuterung methode

Purify the acids as the 2-isomer above, i.e. by distillation, but under a good vacuum. [Prelog & Scherrer Helv Chim Acta 42 2227 1959, Levene & Marker J Biol Chem 93 761 1932, 100 685 1933, Cram J Am Chem Soc 74 2137 1952.] The R-amide crystallises from H2O, with m 101.5-102o, and [] 20 -16.5o (c 1.2, EtOH). The racemic acid has m 39-40o, b 134-136o/6mm, 158o/12mm [Marvel et al. J Am Chem Soc 62 3499 1940]. [Beilstein 9 IV 1813.]

(S)-3-PHENYLBUTYRIC ACID Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


(S)-3-PHENYLBUTYRIC ACID Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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772-15-6()Verwandte Suche:


  • (s)-β-methylhydrocinnamic acid
  • (3S)-3-Phenylbutanoic acid
  • (3S)-3-Phenylbutyric acid
  • (S)-3-Phenylbutanoic acid
  • (2S)-2-Methyl-3-phenylpropanoic acid
  • (S)-3-Phenylisobutyric acid
  • (S)-α-Methylbenzenepropionic acid
  • [S,(+)]-2-Benzylpropionic acid
  • [S,(+)]-2-Methyl-3-phenylpropionic acid
  • (S)-3-PHENYLBUTYRIC ACID
  • (S)-BETA-METHYLHYDROCINNAMIC ACID
  • (S)-3-Phenylbutyric acid >=99.0% (sum of enantiomers, HPLC)
  • 772-15-6
  • Carboxylic acid
  • Chiral Building Blocks
  • Carboxylic Acids
  • Asymmetric Synthesis
  • Organic Building Blocks
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