AKOS B019512

AKOS B019512 Property

Boiling point:

100 °C(Press: 30 Torr)

Density 

1.487 g/mL at 25 °C

refractive index 

1.5214 (estimate)

Flash point:

103 °C

storage temp. 

2-8°C

form 

liquid

pka

0.68±0.10(Predicted)

Appearance

Colorless to light yellow Liquid

InChI

InChI=1S/C5H7BrN2/c1-4-5(6)3-8(2)7-4/h3H,1-2H3

InChIKey

UESOBPUTZLYSGI-UHFFFAOYSA-N

SMILES

N1(C)C=C(Br)C(C)=N1

Safety

Hazard Codes 

Xi

Risk Statements 

37/38-41

Safety Statements 

26-39

HazardClass 

IRRITANT

HS Code 

29331990

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

AKOS B019512 Chemical Properties,Usage,Production

Chemical Properties

White solid

Synthesis

General procedure for the synthesis of 4-bromo-1,3-dimethyl-1H-pyrazole from 1,3-dimethyl-1H-pyrazole: Bromine (2.0 mL, 40.80 mmol) was added slowly and dropwise to a solution of 1,3-dimethyl-1H-pyrazole (3.92 g, 40.80 mmol) in acetic acid (10 mL) at room temperature. The reaction mixture was heated to 70 °C and maintained for 1 hour. Upon completion of the reaction, it was cooled to room temperature and concentrated under vacuum to give the crude product. The pH of the crude product was adjusted with saturated sodium carbonate solution to 7~8. Subsequently, extraction was carried out with ethyl acetate (50 mL x 3), the organic phases were combined and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under vacuum to give the residue. The residue was purified by column chromatography (eluent: ethyl acetate/petroleum ether = 1/6 to 1/4) to afford the target compound 4-bromo-1,3-dimethyl-1H-pyrazole (3.30 g, yield: 46%) as an oil. The product was detected by ESI-MS and showed (M + H)+ peak located at 175.1. 1H NMR (400 MHz, CDCl3) data were as follows: δ 7.30 (s, 1H), 3.83 (s, 3H), 2.23 (s, 3H).

References

[1] J. Gen. Chem. USSR (Engl. Transl.), 1980, vol. 50, # 9, p. 1714 - 1716
[2] Zhurnal Obshchei Khimii, 1980, vol. 50, # 9, p. 2116 - 2119
[3] Patent: WO2015/89327, 2015, A1. Location in patent: Paragraph 0296
[4] Chemische Berichte, 1926, vol. 59, p. 606,1296