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Merck
CN

374822

4-溴吡唑

99%

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关于此项目

经验公式(希尔记法):
C3H3BrN2
化学文摘社编号:
分子量:
146.97
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
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Quality Level

assay

99%

form

solid

bp

250-260 °C (lit.)

mp

93-96 °C (lit.)

functional group

bromo

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-溴吡唑是一种吡唑衍生物。它被报道可与四氯化钛反应生成二元加合物。4-溴吡唑的致突变性已通过使用鼠伤寒沙门氏菌的L-阿拉伯糖正向突变分析进行了检测。据报道,它可抑制氧化磷酸化、ATP-32P交换反应以及能量依赖型和非依赖型的钙摄取。
4-溴吡唑是一种杂芳基卤化物,它在钯催化剂存在下的氰化已被报道。

Application

4-溴吡唑可用于制备4-溴-1-(2-氯乙基)-1H-吡唑。它可作为合成1,4′-双吡唑的起始材料。
通过与二甲基和二乙烯基锡二氯化物反应,4-溴吡唑可用于制备固态的六配位复合物。


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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



全球贸易项目编号

货号GTIN
374822-10G04061832249032
374822-1G04061831834802