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1-Chloro-4-nitrobenzene / 100 G

Purity: 99 %
Synonym: 4-Chloronitrobenzene; p-Nitrochlorobenzene
Molecular Formula: ClC6H4NO2
Molecular Weight: 157.55
SKU: MND-50045
CAS Number: 100-00-5
MDL number: MFCD00007285
EC Number: 202-809-6
Form: crystals
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 100 G  
20.58 EUR



Safety Information


Hazard Statements

H301 + H311 + H331
H373
H411
H351
H341

Precautionary Statements

P202
P280
P301 + P310
P304 + P340 + P311
P273
P302 + P352 + P312

Pictograms



Properties

Signal WordDanger
Flash Point (C)124 °C - closed cup
Flash Point (F)255.2 °F - closed cup
Vapor Density5.4 (vs air)
Vapor Pressure0.09 mmHg ( 25 °C)
Density1.298 g/mL at 25 °C (lit.)
Boiling Point242 °C (lit.)
Melting Point80-83 °C (lit.)

 Product Description

1-Chloro-4-nitrobenzene is a chemical compound consisting of a benzene ring with a chlorine atom and a nitro group attached. It is a pale yellow crystalline solid with a characteristic odor.

 

Application:

This compound is commonly used as an intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and agrochemicals. It serves as a key building block for the synthesis of various aromatic compounds.

 

 

Articles:

- Design and Synthesis of N-Doped Carbons as Efficient Metal-Free Catalysts in the Hydrogenation of 1-Chloro-4-Nitrobenzene

Publication Date: 21 February 2024

Juan-José Villora-Picó, Antonio Sepúlveda-Escribano and María-Mercedes Pastor-Blas

https://doi.org/10.3390/ijms25052515

 

- Structure-activity relationships for chemical and glutathione S-transferase-catalysed glutathione conjugation reactions of a series of 2-substituted 1-chloro-4-nitrobenzenes

Publication Date: DECEMBER 01 1996

Ellen M. VAN der AAR; Tialda BOUWMAN; Jan N. M. COMMANDEUR; Nico P. E. VERMEULEN

https://doi.org/10.1042/bj3200531

 

- Anion activation in the synthesis of ethers from oxygen anions and p-chloronitrobenzene

Publication Date: September 1, 1983

Cristina Paradisi, Ugo Quintily, and Gianfranco Scorrano

https://doi.org/10.1021/jo00166a017