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374822

Sigma-Aldrich

4-Bromopyrazole

99%

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About This Item

Empirický vzorec (Hillův zápis):
C3H3BrN2
Číslo CAS:
2075-45-8
Molekulová hmotnost:
146.97
MDL number:
MFCD00075602
UNSPSC Code:
12352100
PubChem Substance ID:
24863341
NACRES:
NA.22

assay

99%

form

solid

bp

250-260 °C (lit.)

mp

93-96 °C (lit.)

SMILES string

Brc1cn[nH]c1

InChI

1S/C3H3BrN2/c4-3-1-5-6-2-3/h1-2H,(H,5,6)

InChI key

WVGCPEDBFHEHEZ-UHFFFAOYSA-N

General description

4-Bromopyrazole is a heteroaryl halide and its cyanation in the presence of palladium catalysts has been reported.
4-Bromopyrazole is a pyrazole derivative. It is reported to react with titanium tetrachloride to afford binary adducts. Mutagenicity of 4-bromopyrazole has been tested using the L-arabinose forward mutation assay of Salmonella typhimurium. It is reported to inhibit the oxidative phosphorylation, the ATP-32P exchange reaction, and energy dependent and independent calcium uptake.

Application

4-Bromopyrazole may be used in the preparation of 4-bromo-1-(2-chloroethyl)-1H-pyrazole. It may be used as starting material in the synthesis of 1,4′-bipyrazoles.
4-Bromopyrazole may be used in the preparation of solid hexacoordinate complexes by reaction with dimethyl- and divinyl-tindichloride.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Osvědčení o analýze (COA)

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Pyrazole for synthesis

Sigma-Aldrich

8.07572

Pyrazole

1-Boc-pyrazole-4-boronic acid pinacol ester 97%

Sigma-Aldrich

632732

1-Boc-pyrazole-4-boronic acid pinacol ester

1-Methylpyrazole ≥99.0% (GC)

Sigma-Aldrich

91493

1-Methylpyrazole

2-Bromo-1H-imidazole 97%

Sigma-Aldrich

666521

2-Bromo-1H-imidazole

Ilia A. Guzei et al.
Inorganic chemistry, 36(20), 4415-4420 (2001-10-24)
Treatment of titanium tetrachloride with 3,5-di-tert-butylpyrazole affords the complexes [3,5-(C(CH(3))(3))(2)C(3)H(3)N(2)](2)[TiCl(6)] and (3,5-(C(CH(3))(3))(2)C(3)HN(2))(2)TiCl(2) in 37 and 42% yields, respectively. An analogous reaction with 3,5-dimethylpyrazole, 3-methylpyrazole, 4-bromopyrazole, and 4-iodopyrazole leads to the formation of corresponding TiCl(4)L(2) binary adducts in 30-86% yields. Crystal
Kamal Nayan Sharma et al.
Dalton transactions (Cambridge, England : 2003), 42(11), 3908-3918 (2013-01-19)
The reactions of 4-bromo-1-(2-chloroethyl)-1H-pyrazole prepared from 4-bromopyrazole with the in situ generated PhSNa, PhSeNa, Na(2)S and Na(2)Se have resulted in thio/selenoether ligands L1-L4 respectively. The complexes [PdL1/L2Cl(2)](1-2) and [PdL3/L4Cl]BF(4) (3-4) of these ligands have been synthesized by reacting them with
Todd D Senecal et al.
Angewandte Chemie (International ed. in English), 52(38), 10035-10039 (2013-08-13)
Playing it safe: The nontoxic cyanide source K4 [Fe(CN)6]·3H2O can be used for the cyanation of (hetero)aryl halides. The application of palladacycle catalysts prevents poisoning during catalyst formation, thereby allowing for low catalyst loadings, fast reaction times, and wide heterocyclic
Effects of pyrazole, 4-bromopyrazole and 4-methylpyrazole on mitochondrial function.
A I Cederbaum et al.
Biochemical pharmacology, 23(2), 203-213 (1974-01-15)
Dichlorodialkyltin complexes with 4-bromopyrazole. The crystal structure of bis(4-bromopyrazole- N2)dichlorodimethyltin(IV).
Casellato U, et al.
Journal of Organometallic Chemistry, 486(1-2), 105-107 (1995)
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