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2,6-Dichlorophenylhydrazine hydrochloride

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2,6-Dichlorophenylhydrazine hydrochloride Basic information

Product Name:
2,6-Dichlorophenylhydrazine hydrochloride
Synonyms:
  • 2,6-Dichoropheynylhydrazine hydrochloride
  • Hydrazine, (2,6-dichlorophenyl)-, monohydrochloride
  • 6-Dichlorophenylhydrazine hydrochloride
  • (2,6-dichlorophenyl)hydrazine monohydrochloride
  • 2,6-Dichlorophenylhydrazine hydrochloride, 98+%
  • 2,6-DICHLOROPHENYLHYDRAZINE HCL
  • 2,6-DICHLOROPHENYLHYDRAZINE HYDROCHLORIDE
  • 1,3-Dichloro-2-hydrazinobenzene
CAS:
50709-36-9
MF:
C6H7Cl3N2
MW:
213.49
EINECS:
256-730-7
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • Hydrazines
  • Nitrogen Compounds
  • Organic Building Blocks
  • Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
  • API intermediates
Mol File:
50709-36-9.mol
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2,6-Dichlorophenylhydrazine hydrochloride Chemical Properties

Melting point:
225 °C (dec.)(lit.)
Boiling point:
346.49°C (rough estimate)
Density 
1.6100 (rough estimate)
refractive index 
1.6000 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Light yellow to Light orange
BRN 
4569738
CAS DataBase Reference
50709-36-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T,Xi,Xn
Risk Statements 
20/21-25-36/37/38-20/21/22
Safety Statements 
26-36/37/39-45-22
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
6.1
PackingGroup 
HS Code 
29280000

MSDS

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2,6-Dichlorophenylhydrazine hydrochloride Usage And Synthesis

Chemical Properties

white to light yellow powder

Uses

(2,6-Dichlorophenyl)hydrazine Hydrochloride

Uses

2,6-Dichlorophenylhydrazine hydrochloride was used in the preparation of 1-(2,6-dichlorophenyl)-4-methyl-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxylic acid, ethyl ester.

Synthesis

608-31-1

50709-36-9

General procedure for the synthesis of 2,6-dichlorophenylhydrazine hydrochloride from 2,6-dichloroaniline: 2,6-dichloroaniline (10.0 g, 61.72 mmol) was dissolved in an appropriate amount of solvent and cooled to -15 °C. At this temperature, aqueous sodium nitrite (5.11 g, 74.00 mmol) and hydrochloric acid were slowly added. The reaction mixture was stirred at 0-10°C for 15 minutes. The reaction mixture was filtered to remove insoluble matter and subsequently concentrated hydrochloric acid (34.7 g, 150 mmol) was added to the filtrate. The reaction system was maintained at -15 °C and stirring was continued for 30 min, after which the precipitate was collected by filtration to afford 15.00 g of the target product 2,6-dichlorophenylhydrazine hydrochloride. The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 7.18-7.28 (m, 1H), 7.39-7.52 (m, 2H), 10.30 (br s, 3H); the mass spectrum (MS) showed m/z: 176.90 (M)+.

References

[1] Patent: WO2013/186692, 2013, A1. Location in patent: Page/Page column 103; 104

2,6-Dichlorophenylhydrazine hydrochloride Preparation Products And Raw materials

Preparation Products

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