Cyclopentylphenylglykolsure
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- CAS-Nr.
- 427-49-6
- Bezeichnung:
- Cyclopentylphenylglykolsure
- Englisch Name:
- alpha-Cyclopentylmandelic acid
- Synonyma:
- 2-Cyclopentyl-2-hydroxy-2-phenylacetic acid;CYCLOPENTYL MANDELIC ACID;Mandelic acid, alpha-cyclopentyl;Glycopyrronium Bromide EP Impurity J;CM ACID;pha-CycL;TIMTEC-BB SBB010054;2-CYCLOPENTYL MANDELIC ACI;Glycopyrrolate Impurity 15;α-Cyclopentylmandelic acid
- CBNumber:
- CB1751794
- Summenformel:
- C13H16O3
- Molgewicht:
- 220.27
- MOL-Datei:
- 427-49-6.mol
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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
- Löslichkeit
- 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)
Cyclopentylphenylglykolsure Chemische Eigenschaften,Einsatz,Produktion Methoden
R-Sätze Betriebsanweisung:
R34:Verursacht Verätzungen.
S-Sätze Betriebsanweisung:
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, 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
Cyclopentylphenylglykolsure Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Cyclopentylphenylglykolsure Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
Global( 333)Lieferanten
427-49-6(Cyclopentylphenylglykolsure)Verwandte Suche:
- α-Cyclopentyl-DL-Mandelic Acid
- Glycopyrrolate Related CoMpound C
- 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
- α-Cyclopentylmandelic acid
- 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
- CYCLOPENTYL MANDELIC ACID
- 2-Cyclopentyl-2-hydroxy-2-phenylacetic acid
- Glycopyrronium Bromide EP Impurity J
- 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
- Glycopyrronium Bromide Impurity 15
- Glycopyrrolate Related Compound-C / Glycopyrronium Bromide EP impurity J
- 427-49-6
- Building Blocks
- C13 to C42+
- Carbonyl Compounds
- Carboxylic Acids
- Chemical Synthesis
- Organic Building Blocks
- Intermediate
