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146757

2,4-Dichlorobenzaldehyde

Name: 2,4-Dichlorobenzaldehyde
Brand: ALDRICH

99%

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About This Item

Linear Formula:

Cl₂C₆H₃CHO

CAS Number:

874-42-0

Molecular Weight:

175.01

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24848796

EC Number:

212-861-1

Beilstein/REAXYS Number:

471601

MDL number:

MFCD00003305

Assay:

99%

Form:

solid

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Properties

Quality Level

100

assay

99%

form

solid

bp

233 °C (lit.)

mp

64-69 °C (lit.)

functional group

aldehyde, chloro

SMILES string

[H]C(=O)c1ccc(Cl)cc1Cl

InChI

1S/C7H4Cl2O/c8-6-2-1-5(4-10)7(9)3-6/h1-4H

InChI key

YSFBEAASFUWWHU-UHFFFAOYSA-N

Description

General description

2,4-Dichlorobenzaldehyde on condensation with 4-amino-5-mercapto-3-methyl/ethyl-1,2,4-triazole yields bidentate Schiff base ligands and their metal complexes are potential antimicrobial agents.

Application

2,4-Dichlorobenzaldehyde was used in the solid-phase synthesis of a series of indole-based peptoids.

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pictograms

GHS05,GHS09

signalword

Danger

hcodes

H314,H411

pcodes

P260 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

275.0 °F - closed cup

flash_point_c

135 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number

0000467143

0000438843

0000421267

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Metal-based biologically active compounds: synthesis, spectral, and antimicrobial studies of cobalt, nickel, copper, and zinc complexes of triazole-derived schiff bases.

Kiran Singh et al.

Bioinorganic chemistry and applications, 2011, 901716-901716 (2012-01-05)

A series of cobalt, nickel, copper, and zinc complexes of bidentate Schiff bases derived from the condensation reaction of 4-amino-5-mercapto-3-methyl/ethyl-1,2,4-triazole with 2,4-dichlorobenzaldehyde were synthesized and tested as antimicrobial agents. The synthesized Schiff bases and their metal complexes were characterized with

Design and synthesis of indole-based peptoids as potent noncompetitive antagonists of transient receptor potential vanilloid 1.

Martina Quintanar-Audelo et al.

Journal of medicinal chemistry, 50(24), 6133-6143 (2007-11-08)

The vanilloid receptor subunit 1, or transient receptor potential vanilloid 1 (TRPV1), integrates physical and chemical stimuli in the peripheral nervous system, playing a key role in inflammatory pain. Identification of potent TRPV1 antagonists is thus an important goal of

Hybrid compounds from chalcone and 1,2-benzothiazine pharmacophores as selective inhibitors of alkaline phosphatase isozymes.

Adnan Ashraf et al.

European journal of medicinal chemistry, 159, 282-291 (2018-10-09)

Chalcones and 1,2-benzothiazines are two important classes of bioactive compounds, each scaffold endowed with diverse pharmacological activities. Combining both of these pharmacophores in a single molecule was aimed to yield multi-modal agents. Herein, we report a series of hybrid compounds

Global Trade Item Number

SKU	GTIN
146757-100G	04061838737090
146757-5G	04061838737106