(S)-(-)-1-Phenylethanol
CAS No. 1445-91-6
(S)-(-)-1-Phenylethanol( (-)-Methyl phenyl carbinol | (S)-(-)-sec-Phenylethyl alcohol )
Catalog No. M19564 CAS No. 1445-91-6
1-Phenylethanol exists as a solid soluble (in water) and a very weakly acidic compound (based on its pKa).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | 27 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name(S)-(-)-1-Phenylethanol
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NoteResearch use only, not for human use.
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Brief Description1-Phenylethanol exists as a solid soluble (in water) and a very weakly acidic compound (based on its pKa).
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Description1-Phenylethanol exists as a solid soluble (in water) and a very weakly acidic compound (based on its pKa). 1-Phenylethanol has been detected in multiple biofluids such as feces and saliva. Within the cell 1-phenylethanol is primarily located in the cytoplasm.
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In Vitro——
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In Vivo——
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Synonyms(-)-Methyl phenyl carbinol | (S)-(-)-sec-Phenylethyl alcohol
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number1445-91-6
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Formula Weight122.16
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Molecular FormulaC8H10O
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESC[C@H](O)c1ccccc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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VPC-80051 racemate
VPC-80051 is the first small molecule inhibitor of hnRNP A1 splicing activity by using a computer-aided drug discovery approach.
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DSP-0565
DSP-0565 exhibits anti-convulsant activity and good safety margin in various models including scPTZ, 6 Hz, MES, and amygdala kindling.
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PKC ζ pseudosubstrat...
Inhibitor of protein kinase C (PKC) ζ; attached to cell permeabilisation Antennapedia domain vector peptide. Consists of amino acids 113 - 129 of PKC ζ pseudosubstrate domain linked by a disulphide bridge to the Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the inhibitor peptide. Once inside the cell, the disulphide bonds are subjected to reduction in the cytoplasm leading to release of the inhibitor peptide. Induces mast cell degranulation by a PKC ζ-independent pathway.
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