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三溴化吡啶鎓_分子结构_CAS_39416-48-3)
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三溴化吡啶鎓

产品号 A15684 公司名称 Alfa Aesar
CAS号 39416-48-3 公司网站 http://www.alfa.com
分子式 C5H6Br3N 电 话
分子量 319.81984 传 真
纯 度 tech. 90% 电子邮件
保 存 Chembase数据库ID: 111288

产品价格信息

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产品别名

标题
Pyridine hydrobromide perbromide
IUPAC标准名
dibromane pyridine hydrobromide
IUPAC传统名
Brom pyridine hydrobromide
别名
Pyridinium tribromide
Pyridinium bromide perbromide

产品登记号

Beilstein号 3690144
默克索引号 147973
CAS号 39416-48-3
MDL号 MFCD00013223
EC号 254-446-8

产品性质

纯度 tech. 90%
熔点 128-136°C
GHS危险品标识 GHS05
GHS危险声明 H314-H318
欧盟危险性物质标志 腐蚀性(Corrosive) 腐蚀性(Corrosive) (C)
GHS警示性声明 P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501A
危险公开号 34
安全公开号 26-36/37/39-45-60
TSCA收录
联合国危险货物等级 8
联合国危险货物编号 UN3261
联合国危险货物包装类别(PG) III

产品详细信息

参考文献

  • Selective monobromination of anilines, predominantly at the para-position, can be effected in THF: Synth. Commun., 23, 855 (1993). In aqueous AcOH, alkyl aryl ethers are p-brominated in high yield: Synth. Commun., 28, 499 (1998), whereas aryl methyl ethers are demethylated on heating in xylene: Indian J. Chem., 33B, 288 (1994). Cleaves thioacetals in the presence of TBAB: J. Org. Chem., 46, 1745 (1981).
  • Stable, crystalline, readily-handled source of bromine, useful for a wide range of brominations, including ɑ-bromination of ketones: J. Am. Chem. Soc., 70, 417 (1948), and conversion of alkenes to vic-dibromides. See, for example: Org. Synth. Coll., 5, 604 (1973), Note 2. The rate of addition to alkenes increases markedly on increased substitution, so that selective bromination of the more substituted of two double bonds can be achieved: Synthesis, 966 (1979).
  • In pyridine, cyclopentenones are converted directly to their ɑ-bromo derivatives (addition-elimination): Synth. Commun., 18, 1323 (1988).