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Cyclopentylphenylglykolsure

alpha-Cyclopentylmandelic acid Struktur
427-49-6
CAS-Nr.
427-49-6
Bezeichnung:
Cyclopentylphenylglykolsure
Englisch Name:
alpha-Cyclopentylmandelic acid
Synonyma:
2-Cyclopentyl-2-hydroxy-2-phenylacetic acid;CYCLOPENTYL MANDELIC ACID;Glycopyrronium Bromide EP Impurity J;α-Cyclopentylmandelic acid;Mandelic acid, alpha-cyclopentyl;Glycopyrrolate Related CoMpound C;CM ACID;pha-CycL;TIMTEC-BB SBB010054;2-CYCLOPENTYL MANDELIC ACI
CBNumber:
CB1751794
Summenformel:
C13H16O3
Molgewicht:
220.27
MOL-Datei:
427-49-6.mol

Cyclopentylphenylglykolsure Eigenschaften

Schmelzpunkt:
144-150 °C
Siedepunkt:
110 °C (0.5 mmHg)
Dichte
1.247±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
L?slichkeit
Chloroform (Slightly), Methanol (Slightly)
pka
3.53±0.25(Predicted)
Aggregatzustand
Solid
Farbe
White to pale brown
InChI
InChI=1S/C13H16O3/c14-12(15)13(16,11-8-4-5-9-11)10-6-2-1-3-7-10/h1-3,6-7,11,16H,4-5,8-9H2,(H,14,15)
InChIKey
WFLUEQCOAQCQLP-UHFFFAOYSA-N
SMILES
C(C1CCCC1)(C1C=CC=CC=1)(O)C(=O)O
LogP
2.770 (est)
CAS Datenbank
427-49-6(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher C,Xi
R-S?tze: 34-41-37/38
S-S?tze: 45-36/37/39-26-39
RIDADR  3261
WGK Germany  3
HazardClass  IRRITANT
PackingGroup  III
HS Code  29163990
Speicherklasse 11 - Combustible Solids
Hazard Classifications Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Bildanzeige (GHS) Corrosion (GHS05)Exclamation Mark (GHS07)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H318 Verursacht schwere Augensch?den. Schwere Augensch?digung Kategorie 1 Achtung P280, P305+P351+P338, P310
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Cyclopentylphenylglykolsure Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R34:Verursacht Ver?tzungen.

S-S?tze Betriebsanweisung:

S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Chemische Eigenschaften

white to beige powder

Verwenden

intermediate for Glycopyrronium Bromide, Oxyphencyclimine HCl, Oxypyrronium Bromide

Research

Resolving racemic alpha-cyclopentylmandelic acid by a chemical resolution method by using L-Tyrosine methyl ester and (R)-alpha-phenylethylamine as resolution reagents to respectively prepare (S)-alpha-cyclopentylmandelic acid and (R)-alpha-cyclopentylmandelic acid; and carrying out esterification reaction to respectively obtain chiral intermediates (S)/(R)-alpha-cyclopentylmethyl mandelate. Multistage enantioselective liquid-liquid extraction (ELLE) of α--cyclopentyl-mandelic acid (α-CPMA) enantiomers using hydroxyethyl-β-cyclodextrin (HE-β-CD) as extractant was studied in a cascade of centrifugal contactor separators (CCSs)[1].

Cyclopentylphenylglykolsure Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Cyclopentylphenylglykolsure Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 344)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Anhui Dexinjia Biopharm Co., Ltd
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Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070
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427-49-6(Cyclopentylphenylglykolsure)Verwandte Suche:


  • ALPHA-CYCLOPENTYLMANDELIC ACID CM ACID
  • α-Cyclopentylmandelic acid≥ 99% (Titration)
  • alpha-Cyclopentylmandelic acid 97%
  • 2-cyclopentyl-2-hydroxy-2-phenyl-ethanoic acid
  • ALPHA-CYCLOPENTYLMANDELIC ACID
  • CM ACID
  • CYCLOPENTYL-HYDROXY-PHENYL-ACETIC ACID
  • CYCLOPENTYLPHENYLGLYCOLIC ACID
  • TIMTEC-BB SBB010054
  • a-Cyclo Pentyl Mandelic acid
  • 2-CYCLOPENTYL MANDELIC ACID
  • 2-hydroxy-2-cyclopentyl-2-phenylacetic acid
  • α-Cyclopentyl-α-hydroxybenzeneacetic acid
  • alpha-Cyclopentylmandelic acid,98%
  • alpha-Cyclopentyl-DL-mandelic Acid
  • 2-CYCLOPENTYL MANDELIC ACI
  • alpha-CyclopentylMandelic acidCyclopentylphenylglycolic acid
  • Glycopyrrolate Related Compound C (25 mg) (2-Cyclopentyl-2-hydroxy-2-phenylacetic acid)
  • alpha-CyclopentylMandelic acid, 98% 5GR
  • Benzeneacetic acid, a-cyclopentyl-a-hydroxy-
  • alpha-CyclopentylMandelic acid SynonyMs Cyclopentylphenylglycolic acid
  • cyclopentylphenylglycolic acid cyclopentylphenylglycolic acid
  • Glycopyrrolate Impurity 15
  • Glycopyrrolate USP Related Compound C
  • Cyclopentylphenylglykolsure
  • α-Cyclopentyl-DL-mandelic Acid >
  • pha-CycL
  • CMPA =Cyclopentylmandelic acid Purity:98% (2.5 Kg X 3 batches + 3 Kg 4 th batch) 2weeks
  • Glycopyrrolate EP Impurity J
  • Cyclopentyl mandelic acid(Glycopyrrolate Related compound C)
  • TIANFUCHEM--427-49-6--alpha-Cyclopentylmandelic acid
  • α-Cyclopentyl-DL-mandelic Acid
  • Glycopyrrolate Related Compound C (2-Cyclopentyl-2-hydroxy-2-phenylacetic acid) (1296042)
  • alpha-CYCLOPENTYL MANDELIC ACID Extra Pure
  • Mandelic acid, alpha-cyclopentyl
  • Grononium bromide impurity I
  • Benzeneacetic acid, α-cyclopentyl-α-hydroxy-
  • Glycopyrronium Bromide EP Impurity J (Glycopyrrolate USP Related Compound C)
  • 2-Cyclopentyl-2-hydroxyphenylacetic acid
  • Glycopyrrolate Related Compound-C / Glycopyrronium Bromide EP impurity J
  • Glycopyrronium Bromide Impurity
  • Glycopyrronium Bromide Impurity 15
  • 2-(RS)-Cyclopentyl-2-hydroxy-2-phenylacetic Acid (alpha-Cyclopentylmandelic Acid)
  • α-Cyclopentylmandelic acid, CAS 427-49-6
  • alpha-Cyclopentylmandelicaci
  • 2-Cyclopentyl-2-Hydroxy-2-Phenylacetic Acid 2--2-
  • 2-Cyclopentyl-2-hydroxy-2-phenylacetic acid
  • CYCLOPENTYL MANDELIC ACID
  • Glycopyrrolate Related CoMpound C
  • Glycopyrronium Bromide EP Impurity J
  • α-Cyclopentylmandelic acid
  • 427-49-6
  • Building Blocks
  • C13 to C42+
  • Carbonyl Compounds
  • Carboxylic Acids
  • Chemical Synthesis
  • Organic Building Blocks
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