Epoxy curing agent Knowledge 2-Chloro-6-nitrotoluene 2-Chloro-6-nitrotoluene

2-Chloro-6-nitrotoluene 2-Chloro-6-nitrotoluene

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2-Chloro-6-nitrotoluene structural formula

Structural formula

Business number 01TV
Molecular formula C7H6ClNO2
Molecular weight 171.58
label

6-nitro-2-chlorotoluene,

2-Chloro-6-nittoluene,

1-Chloro-2-methyl-3-nitro-benzen,

CH3C6H3(NO2)Cl

Numbering system

CAS number:83-42-1

MDL number:MFCD00007205

EINECS number:201-475-9

RTECS number:XS9130000

BRN number:1239924

PubChem number:24855517

Physical property data

1. Characteristics: needle-like crystals.


2. Density (g/mL,25/4℃): Unsure


3. Relative vapor density (g/mL,AIR=1): Unsure


4. Melting point (ºC): 37 -40℃


5. Boiling point (ºC,Normal pressure):238℃


6. Boiling point (ºC,5.2kPa): Unsure


7. Refractive index:1.537769 ℃)


8. Flashpoint (ºC): 125℃


9. Specific optical rotation (º): Unsure


10. Autoignition point or ignition temperature (ºC): Unsure


11. Vapor pressure (kPa,25ºC): Unsure


12. Molar volume (m3 /mol):129.5


3. isotonic specific volume (90.2K):336.2


4. Surface Tension (dyne/cm):45.4


5. Polarizability10-24cm3):16.85

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: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 45.8

7. Number of heavy atoms: 11

8. Surface charge: 0

9. Complexity: 157

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

None

Storage method

This product should be kept sealed and dry.

Synthesis method

Obtained from the nitration of o-xylene. Cool o-xylene to -10℃, add pre-cooled mixed acid dropwise while stirring (1 portion66%nitric acid2 portion98%sulfuric acid). The dripping temperature is controlled at-10-5℃, add, continue stirring0.5h. Leave to stand to separate the waste acid from the lower layer, take the nitrification solution from the upper layer and use water and water in sequence. 5%Sodium hydroxide solution and water washing, then steam distillation, and then fractionation to obtain3-Nitro-o-xylene. Yield50%.

Purpose

Used as pharmaceutical intermediates .

: 9pt; FONT-FAMILY: 宋体; mso-ascii-font-family: Arial; mso-hansi-font-family: Arial; mso-bidi-font-family: Arial; mso-ansi-language: EN-US; mso -fareast-language: ZH-CN; mso-bidi-language: AR-SA”>℃, add pre-cooled mixed acid dropwise under stirring (1 shares 66%nitric acid2 portion98%formed with sulfuric acid). The dripping temperature is controlled at-10-5℃, add, continue stirring0.5h. Leave to stand to separate the waste acid from the lower layer, take the nitrification solution from the upper layer and use water and water in sequence. 5%Sodium hydroxide solution and water washing, then steam distillation, and then fractionation to obtain3-Nitro-o-xylene. Yield50%.

Purpose

Used as pharmaceutical intermediates .

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Purpose

Used as pharmaceutical intermediates .

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