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4998-15-6

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4998-15-6 Usage

General Description

(4-CHLORO-PHENYL)-OXO-ACETALDEHYDE is a chemical compound with the molecular formula C8H7ClO2. It is a chlorinated derivative of phenylacetaldehyde, which is commonly used in the synthesis of pharmaceuticals and agrochemicals. (4-CHLORO-PHENYL)-OXO-ACETALDEHYDE has a distinctive aromatic odor and is often used as an intermediate in the production of various organic compounds. It is important to handle (4-CHLORO-PHENYL)-OXO-ACETALDEHYDE with caution, as it can be harmful if ingested, inhaled, or comes into contact with the skin. Additionally, it should be stored and disposed of properly to avoid any environmental contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 4998-15-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4998-15:
(6*4)+(5*9)+(4*9)+(3*8)+(2*1)+(1*5)=136
136 % 10 = 6
So 4998-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClO2/c9-7-3-1-6(2-4-7)8(11)5-10/h1-5H

4998-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-CHLORO-PHENYL)-OXO-ACETALDEHYDE

1.2 Other means of identification

Product number -
Other names p-Cl-phenylglyoxal

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:4998-15-6 SDS

4998-15-6Relevant articles and documents

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Karrer,Musante

, p. 1140,1142 (1935)

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An efficient synthesis of polyfunctionalized pyrroles by three-component reaction of arylglyoxals, Meldrum’s acid and ethyl 2-chloro-3-(arylamino)but-2-enoates

Anary-Abbasinejad, Mohammad,Nezhad-shahrokhabadi, Fereshteh

, (2022/01/19)

A fast and convenient method for synthesis of some new functionalized pyrrole derivatives have been described via a three-component reaction between arylglyoxals, Meldrum’s acid and ethyl 2-chloro-3-(arylamino)but-2-enoate derivatives in excellent yields.

One-pot synthesis of stable phosphorus ylides by three-component reaction between arylglyoxals, phosphines and barbituric or Meldrum’s acid

Latifi, Mahsa,Anary-Abbasinejad, Mohammad

, p. 133 - 139 (2022/01/28)

An efficient one-pot method for the synthesis of new substituted phosphorus ylides is described via three-component reaction between arylglyoxals, C–H acids such as barbituric acid and Meldrum’s acid and triphenylphosphine or tri-n-octylphosphine. This re

A novel class for carbonic anhydrases inhibitors and evaluation of their non-zinc binding

Kuzu, Burak,Tan, Meltem,Gül?in, ?lhami,Menges, Nurettin

, (2021/06/09)

In this study, 23 different imidazole derivatives were synthesized, and the inhibitory properties of these derivatives against carbonic anhydrase I and II isoenzymes were investigated for the first time. The inhibition concentrations of the imidazole derivatives were found to be in the range of 2.89–115.5 nM. Docking studies examined the binding properties of the imidazole derivatives, and the structure–activity relationship is discussed. Theoretical calculations showed that the binding mode of the imidazole ring was non-zinc binding.

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