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41593

Sigma-Aldrich

2-Ethoxy-2-(2-naphthyl)acetonitrile

≥95.0% (HPLC)

Synonym(s):

α-Ethoxy-2-naphthaleneacetonitrile

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About This Item

Empirical Formula (Hill Notation):
C14H13NO
CAS Number:
Molecular Weight:
211.26
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

Assay

≥95.0% (HPLC)

fluorescence

λex 227 nm; λem 336 nm in methanol

SMILES string

CCOC(C#N)c1ccc2ccccc2c1

InChI

1S/C14H13NO/c1-2-16-14(10-15)13-8-7-11-5-3-4-6-12(11)9-13/h3-9,14H,2H2,1H3

InChI key

SERAXWXRCADJHK-UHFFFAOYSA-N

Application

2-Ethoxy-2-(2-naphthyl)acetonitrile is a fluorogenic substrate for use in cytochrome P450 assays.

Pictograms

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

41593-5MG-F:
41593-VAR-F:
41593-BULK-F:


Certificates of Analysis (COA)

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Alexander Zawaira et al.
Current drug metabolism, 12(7), 684-700 (2011-07-12)
The original map of mammalian cytochrome P450 (CYP450) residues involved in substrate recognition was prepared for the CYP2 family by Gotoh in 1992 by manual alignment of mammalian CYP450 residues with substrate recognition site (SRS) residues manually delimited from a
David S Wishart
Drugs in R&D, 8(6), 349-362 (2007-10-30)
Drug development is an intrinsically risky business. Like a high stakes poker game the entry costs are high and the probability of winning is low. Indeed, only a tiny percentage of lead compounds ever reach US FDA approval. At any
Alexander Zawaira et al.
Pharmacogenetics and genomics, 18(6), 467-476 (2008-05-23)
We have used maximum-likelihood models of codon substitution to investigate the role of adaptive evolution in the evolution of cytochrome P450 (CYP) sequences. Evidence for the operation of adaptive evolution in the evolution of rat CYP2C, rabbit CYP2C, rat CYP2D

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