ChemicalBook--->CAS DataBase List--->6575-27-5

6575-27-5

6575-27-5 Structure

6575-27-5 Structure
IdentificationMore
[Name]

2,6-Dichlorobenzylamine
[CAS]

6575-27-5
[Synonyms]

2,6-DICHLOROBENZYLAMINE
RARECHEM AL BW 0148
SALOR-INT L480827-1EA
TIMTEC-BB SBB003780
(2,6-dichlorophenyl)methanamine
2,6-Dichlorobenzylamine, 97+%
[Molecular Formula]

C7H7Cl2N
[MDL Number]

MFCD00047928
[Molecular Weight]

176.04
[MOL File]

6575-27-5.mol
Chemical PropertiesBack Directory
[Appearance]

Clear pale yellow liquid
[Melting point ]

40°C
[Boiling point ]

108°C/ 8mm
[density ]

1.320±0.06 g/cm3(Predicted)
[refractive index ]

1.557-1.559
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Liquid
[pka]

7.98±0.10(Predicted)
[color ]

Clear colorless to yellow
[Sensitive ]

Air Sensitive
[CAS DataBase Reference]

6575-27-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

R34:Causes burns.
[Safety Statements ]

S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[RIDADR ]

UN2735
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29214990
Hazard InformationBack Directory
[Chemical Properties]

Clear pale yellow liquid
[Uses]

(2,6-Dichlorophenyl)methanamine was one of the reactants used in making a library of highly selective and potent G protein-coupled receptor kinase 2 inhibitors.
[Synthesis]

2,6-Dichlorobenzaldoxime

25185-95-9

2,6-Dichlorobenzylamine

6575-27-5

The general procedure for the synthesis of 2,6-dichlorobenzaldehyde oxime as raw material for 2,6-dichlorobenzylamine was as follows: 2,6-dichlorobenzaldehyde oxime (0.121 g, 1 mmol) was mixed and milled with nano Fe3O4 (0.046 g, 0.2 mmol, particle size about 70 nm) in a porcelain mortar. Subsequently, ZrCl4 (0.233 g, 1 mmol) was added and the mixture continued to be ground at room temperature. The mortar was heated in an oil bath until the temperature of the reaction mixture reached 75-80 °C. After batchwise addition of NaBH3CN (0.314 g, 5 mmol), the reaction mixture was continued to be ground at 75-80 °C for 15 min. After the reaction was completed, H2O (5 mL) was added and stirred for 5 min. The mixture was extracted with EtOAc (2 x 5 mL), the organic phases were combined and dried with anhydrous Na2SO4. Evaporation of the solvent gave a pure 2,6-dichlorobenzylamine liquid in 93% yield (0.1 g, see Table 2, entry 1).

[References]

[1] Journal of the Iranian Chemical Society, 2015, vol. 12, # 5, p. 873 - 878
[2] Journal of Medicinal Chemistry, 1984, vol. 27, # 9, p. 1111 - 1118
Spectrum DetailBack Directory
[Spectrum Detail]

2,6-Dichlorobenzylamine(6575-27-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2,6-Dichlorobenzylamine, 98%(6575-27-5)
[Alfa Aesar]

2,6-Dichlorobenzylamine, 97+%(6575-27-5)
[Sigma Aldrich]

6575-27-5(sigmaaldrich)
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