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三聚氟氰

产品号 A15666 公司名称 Alfa Aesar
CAS号 675-14-9 公司网站 http://www.alfa.com
分子式 C3F3N3 电 话
分子量 135.0474096 传 真
纯 度 98% 电子邮件
保 存 Chembase数据库ID: 126782

产品价格信息

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产品别名

标题
Cyanuric fluoride
IUPAC标准名
trifluoro-1,3,5-triazine
IUPAC传统名
cyanuric fluoride
别名
2,4,6-Trifluoro-1,3,5-triazine

产品登记号

EC号 211-620-8
MDL号 MFCD00014597
Beilstein号 124237
CAS号 675-14-9

产品性质

纯度 98%
沸点 73-74°C
密度 1.574
熔点 -38°C
折射率 1.3840
GHS危险品标识 GHS05
GHS危险品标识 GHS06
GHS危险声明 H310-H330-H314-H318
欧盟危险性物质标志 剧毒(Highly toxic) 剧毒(Highly toxic) (T+)
GHS警示性声明 P260-P303+P361+P353-P304+P340-P305+P351+P338-P320-P361-P405-P501A
危险公开号 24-26-35
RTECS编号 XZ1750000
安全公开号 20-26-27/28-36/37/39-45
保存注意事项 Moisture Sensitive
TSCA收录
联合国危险货物等级 6.1
联合国危险货物编号 UN3389
联合国危险货物包装类别(PG) I

产品详细信息

参考文献

  • In combination with pyridine, converts carboxylic acids to acyl fluorides in high yields under mild conditions: Synthesis, 487 (1973). Similarly, protected (Fmoc) amino acids are converted in dichloromethane solution to amino acid fluorides. tert-Butyl ester and ether groups are also stable under these conditions. The resulting acyl fluorides are more stable to water than the corresponding acyl chlorides but are more reactive to amines, thus providing a useful peptide coupling method: J. Am. Chem. Soc., 112, 9651 (1990); Tetrahedron, 50, 5309 (1994); Appendix 6. For use of Fmoc amino acid fluorides in solid-phase peptide synthesis, see: Tetrahedron Lett., 32, 1303 (1991); J. Org. Chem., 59, 3275 (1994). For a review of peptide synthesis via amino acid halides, see: Acc. Chem. Res., 29, 268 (1996).
  • Carboxylic acids can be converted to alcohols under mild conditions via the acyl fluoride and reduction with NaBH4 in the presence of MeOH. The method can be carried out in one pot and is applicable to N-protected amino acids and peptides for which other reduction methods are unsuitable: J. Org. Chem., 61, 6994 (1996).
  • Reagent for deoxygenation of alkyl sulfoxides, cf Cyanuric chloride, L03442: Synthesis, 221 (1980), and for dehydration, at room temperature in DMF, of Boc amino acid amides to nitriles: Tetrahedron. Lett., 38, 4221 (1997).