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173282-69-4

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173282-69-4 Usage

General Description

6-Phenoxynicotinaldehyde, also known as 6-phenoxy nicotinaldehyde or 4819-77-6, is a chemical compound that is primarily used in the production of pharmaceuticals and organic intermediates. It falls under the categories of aldehyde, aliphatic, aromatic, and heterocyclic organic compounds. As a compound that's not naturally occurring, it is usually created synthetically in a laboratory setting. It is essential for researchers to handle this chemical carefully due to its reactivity and potential hazards. Specific safety data and information about the possible impacts of this chemical on environmental and human health are not readily available and it requires careful handling and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 173282-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,2,8 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 173282-69:
(8*1)+(7*7)+(6*3)+(5*2)+(4*8)+(3*2)+(2*6)+(1*9)=144
144 % 10 = 4
So 173282-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO2/c14-9-10-6-7-12(13-8-10)15-11-4-2-1-3-5-11/h1-9H

173282-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Phenoxynicotinaldehyde

1.2 Other means of identification

Product number -
Other names 6-phenoxypyridine-3-carbaldehyde

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:173282-69-4 SDS

173282-69-4Relevant articles and documents

Abnormal Nucleophilic Substitution in 3-Trichloromethylpyridine, its N-Oxide and 3,5-Bis(trichloromethyl)pyridine

Cartwright, David,Ferguson, John R.,Giannopoulos, Thomas,Varvounis, George,Wakefield, Basil J.

, p. 12791 - 12796 (1995)

The scope of abnormal reactions of nucleophiles with β-trichloromethylazines is further explored: reactions of 3-trichloromethylpyridine with nucleophiles other than methoxide, and reactions of 3-trichloromethylpyridine N-oxide and 3,5-bis(trichloromethyl)pyridine with methoxide.Attack at a ring carbon, followed by hydrogen migration to the side-chain, occured in most cases, though attack at the trichloromethyl carbon was also sometimes observed.

HETEROCYCLIC COMPOUNDS AS MUTANT IDH INHIBITORS

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Paragraph 0456-0457, (2020/07/16)

The present disclosure relates generally to compounds useful in treatment of conditions associated with mutant isocitrate dehydrogenase (mt-IDH), particularly mutant IDH1 enzymes. Specifically, the present invention discloses compound of formula (IA), which exhibits inhibitory activity against mutant IDH1 enzymes. Method of treating conditions associated with excessive activity of mutant IDH1 enzymes with such compound is disclosed. Uses thereof, pharmaceutical composition, and kits are also disclosed.

Pymetrozine derivative and its preparation method and application of parasite killing

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Sheet 0031; 0032; 0033; 0034, (2018/07/07)

The invention relates to a pymetrozine derivative (I) and a preparing method and insecticidal application thereof. According to a formula of the pymetrozine derivative (I), groups' meanings are shown in an instruction. The pymetrozine derivative (I) has excellent activity of killing aphids and insecticidal activity of killing mosquito larvae, cotton bollworms, European corn borers and armyworms.

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