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66217-26-3

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66217-26-3 Usage

Derivative of

Naphthalene

Common uses

Synthesis of pharmaceuticals and agrochemicals

Physical properties

Color: Colorless to yellow
Odor: Strong aromatic
Solubility: Insoluble in water, soluble in most organic solvents

Hazards

Can cause irritation to skin, eyes, and respiratory system upon exposure
Should be handled with care

Check Digit Verification of cas no

The CAS Registry Mumber 66217-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,1 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66217-26:
(7*6)+(6*6)+(5*2)+(4*1)+(3*7)+(2*2)+(1*6)=123
123 % 10 = 3
So 66217-26-3 is a valid CAS Registry Number.

66217-26-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethoxynaphthalene-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Ethoxy-6-cyanonaphthalene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66217-26-3 SDS

66217-26-3Downstream Products

66217-26-3Relevant articles and documents

Discovery of a sensitive, selective, and tightly binding fluorogenic substrate of bovine plasma amine oxidase

Ling, Ke-Qing,Sayre, Lawrence M.

supporting information; experimental part, p. 339 - 350 (2009/04/11)

(Chemical Equation Presented) We report a novel fluorogenic substrate of bovine plasma amine oxidase (BPAO), namely, (2-(6-(aminomethyl)naphthalen-2- yloxy)ethyl)trimethylammonium (ANETA), which displays extremely tight binding to BPAO (Km 183 ± 14 nM) and yet is metabolized fairly quickly (kcat 0.690 ± 0.010 s-1), with the aldehyde turnover product (2-(6-formylnaphthalen-2-yloxy)ethyl)trimefhylammonium serving as a real time reporting fluorophore of the enzyme activity. This allowed for the development of a fluorometric noncoupled assay that is 2 orders of magnitude more sensitive than the spectrophotometric benzylamine assay. The discovery of ANETA involved elaboration of the lead compound 6-methoxy-2-naphthalene- methaneamine by structure-based design, which recognized the ancillary cation binding site of BPAO as the most significant structural features controlling binding affinity. Structure-based design further ensured a high level of selectivity: ANETA is a good substrate of BPAO but is not a substrate of either porcine kidney diamine oxidase (pkDAO) or rat liver monoamine oxidase (MAO-B). ANETA represents the first highly sensitive, selective, and tight binding fluorogenic substrate of a copper amine oxidase that is able to respond directly to the enzyme activity in real time.

Synthetic inhibitors of serine proteinases

Wagner,Lischke,Markwardt,et al.

, p. 761 - 763 (2007/10/05)

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