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140681-55-6 分子结构
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1-(chloromethyl)-4-fluoro-1,4-diazabicyclo[2.2.2]octane-1,4-diium; bis(tetrafluoroboranuide)

ChemBase编号:7710
分子式:C7H14B2ClF9N2
平均质量:354.2600888
单一同位素质量:354.08879092
SMILES和InChIs

SMILES:
[N+]12(CC[N+](CCl)(CC1)CC2)F.[B-](F)(F)(F)F.[B-](F)(F)(F)F
Canonical SMILES:
F[B-](F)(F)F.F[B-](F)(F)F.ClC[N+]12CC[N+](CC1)(CC2)F
InChI:
InChI=1S/C7H14ClFN2.2BF4/c8-7-10-1-4-11(9,5-2-10)6-3-10;2*2-1(3,4)5/h1-7H2;;/q+2;2*-1
InChIKey:
TXRPHPUGYLSHCX-UHFFFAOYSA-N

引用这个纪录

CBID:7710 http://www.chembase.cn/molecule-7710.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
1-(chloromethyl)-4-fluoro-1,4-diazabicyclo[2.2.2]octane-1,4-diium; bis(tetrafluoroboranuide)
4-(chloromethyl)-1-fluoro-1,4-diazabicyclo[2.2.2]octane-1,4-diium; bis(tetrafluoroboranuide)
IUPAC传统名
1-(chloromethyl)-4-fluoro-1,4-diazabicyclo[2.2.2]octane-1,4-diium ditetrafluoroborate
4-(chloromethyl)-1-fluoro-1,4-diazabicyclo[2.2.2]octane-1,4-diium ditetrafluoroborate
别名
1-氯甲基-4-氟-1,4-二氮杂双环[2.2.2]辛烷二(四氟硼酸)盐
1-氯甲基-4-氟-1,4-二氮杂双环[2.2.2]辛烷二(四氟硼酸)盐
N-氯甲基-N′-氟三乙二铵双(四氟硼酸盐)
Selectfluor® 氟化剂
1-氯甲基-4-氟-1,4-重氮化二环2.2.2辛烷双(四氟硼酸盐)
1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
F-TEDA
1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
N-Chloromethyl-N′-fluorotriethylenediammonium bis(tetrafluoroborate)
Selectfluor® fluorinating reagent
N-Fluoro-N'-chloromethyltriethylenediamine bis(tetrafluoroborate)
Selectfluor
1-(Chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
1-(Chloromethyl)-4-fluoro-1,4-diazabicyclo[2.2.2]octane-1,4-diium tetrafluoroborate
F-TEDA-BF4
SELECTFLUOR Fluorinating Reagent
CAS号
140681-55-6
EC号
414-380-4
MDL号
MFCD00142607
Beilstein号
5368649
PubChem SID
160971017
24867509
PubChem CID
2724933

理论计算性质

理论计算性质

JChem
质子受体 质子供体
LogD (pH = 5.5) -4.414943  LogD (pH = 7.4) -4.414943 
Log P -4.414943  摩尔折射率 56.7255 cm3
极化性 16.74862 Å3 极化表面积 0.0 Å2
可自由旋转的化学键 里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 产品相关信息 生物活性(PubChem)
熔点
250°C dec expand 查看数据来源
260 °C(lit.) expand 查看数据来源
260°C expand 查看数据来源
ca 250°C dec. expand 查看数据来源
保存注意事项
IRRITANT, KEEP COLD, SELF-HEATING SOLID expand 查看数据来源
Self-Heating/Harmful/Corrosive/Moisture Sensitive/Store under Argon/Keep Cold expand 查看数据来源
欧盟危险性物质标志
X expand 查看数据来源
有害性(Harmful) 有害性(Harmful) (Xn) expand 查看数据来源
联合国危险货物编号
3088 expand 查看数据来源
UN3088 expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
2 expand 查看数据来源
联合国危险货物等级
4.2 expand 查看数据来源
联合国危险货物包装类别(PG)
2 expand 查看数据来源
II expand 查看数据来源
危险公开号
22-41-43-52/53 expand 查看数据来源
安全公开号
21-26-36/37/39-61 expand 查看数据来源
TSCA收录
true expand 查看数据来源
expand 查看数据来源
GHS危险品标识
GHS02 expand 查看数据来源
GHS05 expand 查看数据来源
GHS07 expand 查看数据来源
GHS警示词
Danger expand 查看数据来源
GHS危险声明
H252-H302-H317-H318-H412 expand 查看数据来源
H302-H317-H318-H412 expand 查看数据来源
H318-H302-H317-H313-H402-H412 expand 查看数据来源
GHS警示性声明
P235 + P410-P273-P280-P305 + P351 + P338 expand 查看数据来源
P261-P280-P273-P270-P305+P351+P338 expand 查看数据来源
P273-P280-P305 + P351 + P338 expand 查看数据来源
个人保护装置
dust mask type N95 (US), Eyeshields, Faceshields, Gloves expand 查看数据来源
RID/ADR
UN 3088 4.2/PG 2 expand 查看数据来源
保存温度
2-8°C expand 查看数据来源
纯度
≥97.0% (NMR) expand 查看数据来源
95+% expand 查看数据来源
98+% expand 查看数据来源
浓度
>95% in F+ active expand 查看数据来源
级别
purum expand 查看数据来源
适用性
in accordance for 19F-, 1H-NMR expand 查看数据来源
Empirical Formula (Hill Notation)
C7H14B2ClF9N2 expand 查看数据来源

详细说明

详细说明

Apollo Scientific Apollo Scientific Sigma Aldrich Sigma Aldrich
Apollo Scientific Ltd -  PC3728K external link
Electrophilic fluorinating agent. Ask for technical literature(SelectfluorR - Registered trademark of Air Products). Decomposes exothermally at >1000C
Sigma Aldrich -  439479 external link
Application
亲电氟的高效多功能源。
引起 2,5-二芳基呋喃氧化开环生成顺式-1,4-烯二酮的氟化剂。2还用于硅烯酮缩醛直接氟化生成 α-氟-α-芳基羧酸。3
用于制备氟化酰基硅烷的亲电氟化剂。?
包装
5, 25, 100 g in poly bottle
Citation
综述。1
法律信息
Selectfluor 注册商标 Air Products & Chemicals, Inc.
Sigma Aldrich -  25140 external link
Other Notes
亲电氟化1,2,3试剂;选择性氧化剂4

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • SELECTFLUOR is a registered trademark of Air Products & Chemicals Inc.
  • Stabilized carbanions can be selectively mono- or difluorinated: J. Chem. Soc., Chem. Commun., 343 (1994); Tetrahedron, 51, 3587 (1995). Fluorinated steroids have been prepared from enol acetates or silyl enol ethers: J. Org. Chem., 58, 2791 (1993). 5-Fluoropyrimidine nucleosides can be obtained by treatment of protected nucleosides with the reagent in the presence of water or methanol, followed by elimination of the resulting fluorohydrin derivative: J. Org. Chem., 60, 7340 (1995).
  • For application to N-fluorination of amines, see: Chem. Commun., 1196 (2001). Review of mechanistic insight and applications of the reagent: Angew. Chem. Int Ed., 44, 192 (2005).Brief feature on uses in synthesis: Synlett, 807 (2006). Review of electrophilic N-F fluorinating agents: Chem. Rev., 96, 1737 (1996).
  • Water- and organic-soluble reagent developed by R. E. Banks and co-workers for electrophilic fluorination of a variety of substrates under mild conditions: USP 5,086,178 (1992 to Air Products & Chemicals, Inc.); review: J. Fluorine Chem., 87, 1 (1998). In acetonitrile, activated aromatics can be fluorinated in good yield: J. Chem. Soc., Perkin 1., 2069 (1996). Less active substrates can be fluorinated in the presence of triflic acid: Israel J. Chem., 39, 207 (1999). In acetonitrile, vinylsilanes undergo fluorodesilylation to give vinyl fluorides with retention of configuration: Chem. Commun., 233 (2001).
  • For use in the synthesis of fluorinated carbohydrates by reaction with glycals, see: J. Am. Chem. Soc., 119, 11743 (1997); J. Org. Chem., 64, 5264 (1999).
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专利

专利

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