Toluene diisocyanate manufacturer Knowledge p-Nitrobenzoyl chloride p-Nitrobenzoyl chloride

p-Nitrobenzoyl chloride p-Nitrobenzoyl chloride

Structural formula of p-nitrobenzoyl chloride

Structural formula

Business number 03EG
Molecular formula C7H4ClNO3
Molecular weight 185.56
label

4-nitrobenzoyl chloride,

p-nitrobenzoyl chloride,

p-nitrobenzoyl chloride,

Nitroxyl,

P-nitrobenzoyl chloride,

4-nitrobenzoyl chloride p-nitrobenzoyl chloride,

p-nitrobenzoyl chloride,

4-Nitrobenzoyl chloride,

4-Nitrobenzoic acid chloride,

Labotest-Bb Lt00077260,

P-Nitrobenzoyl Chloride,

Nitrobenzoyl-4 chloride,

4-Nitro-benzoylchlorid,

Benzoyl chloride, 4-nitro-,

Benzoyl chloride, p-nitro-,

catalyst,

additives,

chemical additives

Numbering system

CAS number:122-04-3

MDL number:MFCD00007345

EINECS number:204-517-4

RTECS number:DM6651000

BRN number:473192

PubChem number:24886509

Physical property data

1. Properties: Bright yellow needle-like crystals, with a pungent odor, easy to deliquesce, and decompose when exposed to water and alcohol.

2. Melting point (℃): 72~75℃

3. Boiling point (ºC): 205℃/14kPa, 154℃/1.5kPa

4 .         Solubility: Soluble in ether

Toxicological data

1. Acute toxicity: Rat oral LD50: 5600mg/kg

Mouse oral LC50: 3440mg/kg

Rabbit oral LD50: 4750mg/kg

p>

2. Other multiple dose toxicity: Oral TDLO in rats: 16800mg/kg/30D-I

Unknown mammal inhalation TCLO: 11830ug/m3/ 4H/17W-I

3. Reproductive toxicity: Unknown mammal (male, before mating) inhalation TCLO: 11830ug/m3/4H/16W

4. Mutagenic toxicity: Salmonella microbial mutation test system: 3ug/plate

Ecological data

None

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 43.04

2. Molar volume (cm3/mol): 127.6

3. Isotonic specific volume (90.2K): 346.5

4. Surface tension (dyne/cm): 54.2

5. Dielectric constant:

6�� Dipole moment (10-24cm3):

7, Polarizability: 17.06

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: none

6. Topological molecule polar surface area 62.9

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 193

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Toxic! It is corrosive and can cause burns.

2. Irritating to the respiratory system.

Storage method

1. Storage

Storage in sealed and dry packaging.

Synthesis method

1. This product can be produced by using p-nitrobenzoic acid as raw material and chlorination with thionyl chloride, phosphorus oxychloride or phosgene. P-nitrobenzoic acid and phosphorus oxychloride are heated and refluxed for 24 hours, and phosphorus oxychloride is recovered under reduced pressure to generate p-nitrobenzoyl chloride. Or heat p-nitrobenzoic acid and thionyl chloride to 90°C, reflux for 30-40 hours, and then cool to precipitate p-nitrobenzoyl chloride crystals. The yield is 90%. By passing phosgene into molten p-nitrobenzoic acid and distilling the phosgenation reactant under reduced pressure, p-nitrobenzoyl chloride can also be obtained.

2.Place dry p-nitrobenzoic acid and phosphorus pentachloride in an oil bath and heat until the reaction is complete, then recover under reduced pressure Phosphorus oxychloride. Then, vacuum distillation is used to evaporate the residue to obtain the crude product. After melting the crude product, add carbon tetrachloride, filter while it is hot, and cool and crystallize to obtain the finished product.
The process equation is:

Purpose

1. Mainly used for the synthesis of cephazolin, procaine and folic acid. It is also widely used as an intermediate for dyes and pesticides.

2. Used in the determination of alcohols and phenols, dye manufacturing, pharmaceutical industry, and as an intermediate for color developers.

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/25535

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