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1,1'-羰基二咪唑_分子结构_CAS_530-62-1)
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1,1'-羰基二咪唑

产品号 A14688 公司名称 Alfa Aesar
CAS号 530-62-1 公司网站 http://www.alfa.com
分子式 C7H6N4O 电 话
分子量 162.14874 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 8903

产品价格信息

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产品别名

标题
1,1'-Carbonyldiimidazole
IUPAC标准名
1-(1H-imidazole-1-carbonyl)-1H-imidazole
IUPAC传统名
carbonyldiimidazole
别名
CDI

产品登记号

EC号 208-488-9
CAS号 530-62-1
默克索引号 141819
MDL号 MFCD00005286
Beilstein号 6826

产品性质

纯度 97%
熔点 116-120°C
GHS危险品标识 GHS05
GHS危险品标识 GHS06
GHS危险声明 H301-H314-H318
欧盟危险性物质标志 X
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-P301+P310-P303+P361+P353-P305+P351+P338-P405-P501A
危险公开号 22-34
安全公开号 26-36/37/39-45
保存注意事项 Moisture Sensitive
TSCA收录
联合国危险货物等级 8
联合国危险货物编号 UN3263
联合国危险货物包装类别(PG) II

产品详细信息

参考文献

  • Reagent for peptide coupling via the acylimidazolide: Liebigs Ann. Chem., 609, 75 (1957); J. Am. Chem. Soc., 80, 4423 (1958); 82, 4596 (1960): J. Org. Chem., 27, 2094 (1962). For peptide reagents, see Appendix 6.
  • One-pot esterification of a carboxylic acid with t-BuOH occurs in the presence of DBU: Synthesis, 833 (1982). The reactivity of acyl imidazolides can be increased by N-alkylation: Chem. Pharm. Bull., 32, 5044 (1984).
  • Acylimidazolides can also be reduced to aldehydes by DIBAL-H. This reaction has been applied to N-protected amino acids: J. Chem. Soc., Chem. Commun., 79 (1979).
  • Dehydrates aldoximes, including chiral oximes, to nitriles in high yield: J. Chem. Soc., Chem. Commun., 628 (1973); Synth. Commun., 12, 25 (1982). Ketoximes can be converted to amides by the spontaneous Beckmann rearrangement of imidazolium salts: Chem. Pharm. Bull., 32, 2560 (1984):
  • ?-Hydroxy amino acids are dehydrated to dehydroamino acids: Synthesis, 968 (1982).
  • ɑ?-Dihydroxyketones are converted toɑ-diketones: Synth. Commun., 23, 2219 (1993).