4-碘苯甲腈 | 3058-39-7
中文名称:
4-碘苯甲腈
英文名称:
4-Iodobenzonitrile
CAS No.:
3058-39-7
分子式:
C7 H4 NI
分子量:
229.01736
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:4-碘苯甲腈结构式
名称和标识符
MDL
MFCD00051310
InChIKey
XOKDXPVXJWTSRM-UHFFFAOYSA-N
Inchi
InChI=1S/C7H4IN/c8-7-3-1-6(5-9)2-4-7/h1-4H
SMILES
N#CC1=CC=C(I)C=C1
别名信息
- 中文别名 -
4-碘苯甲腈
4-碘氰基苯
对碘苯腈
4-碘苯基氰
4-碘苯腈
3-甲氧基-4-甲基苯乙腈
4-Iodobenzonitrile 4-碘苯甲腈
4-碘苄腈
对碘苯甲腈
1-氰基-4-碘苯
- 英文别名 -
4-Iodobenzonitrile
-4-IODOBENZONITRILE
P-IODOBENZONITRILE
4-iodo-benzonitril
Benzonitrile, p-iodo-
p-Cyanoiodobenzene
4-Cyanoiodobenzene
4-IODO-1-CYANOBENZENE
1-Cyano-4-iodobenzene
4-Cyanophenyl iodide
4-Iodocyanobenzene
p-Cyanophenyl iodide
1-Iodo-4-cyanobenzene
4-iodbenzonitril
Benzonitrile,4-iodo
Benzonitrile,p-iodo
para-iodobenzonitrile
p-Iodobenzonitrile
4-Iodobenzonitrile, 97%
CL8216
FT-0634624
MFCD00051310
p-iodo-benzonitrile
4-CYANOIODOBENZENE
Benzonitrile, 4-iodo-
NS00028943
J-018030
AM20040140
FT-0656489
PS-7742
SY016999
EN300-67216
3058-39-7
p-Jodbenzonitril
CS-W009114
I0661
DTXSID3062819
NSC 87894
NSC-87894
4-iodo-benzonitrile
AC-22944
J-515571
Z57899725
NSC87894
AKOS005146080
DS-1568
SCHEMBL82069
4-Iodobenzonitrile,98%
物化性质
实验特性
LogP
2.16288
PSA
23.79000
折射率
1.66
水溶性
Insoluble in water.
沸点
271.6 °C at 760 mmHg
熔点
124-128 °C (lit.)
闪点
118℃
颜色与性状
无可用
溶解性
无可用
敏感性
Light Sensitive
密度
1.9241 (estimate)
计算特性
精确分子量
228.93900
氢键供体数量
0
氢键受体数量
1
可旋转化学键数量
0
同位素质量
228.939
重原子数量
9
复杂度
127
同位素原子数量
0
确定原子立构中心数量
0
不确定原子立构中心数量
0
确定化学键立构中心数量
0
不确定化学键立构中心数量
0
共价键单元数量
1
疏水参数计算参考值(XlogP)
无
互变异构体数量
无
表面电荷
0
拓扑分子极性表面积
23.8A^2
海关数据
海关编码
2926909090
海关数据
中国海关编码:
2926909090
概述:
2926909090 其他腈基化合物. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:6.5% 普通关税:30.0%
申报要素:
品名, 成分含量, 用途
Summary:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
相关文献
1.
A photoresponsive palladium complex of an azopyridyl-triazole ligand: light-controlled solubility drives catalytic activity in the Suzuki coupling reaction
Attila Kunfi,István Jablonkai,Tamás Gazdag,Péter J. Mayer,Péter Pál Kalapos,Krisztina Németh,Tamás Holczbauer,Gábor London RSC Adv. 2021 11 23419
2.
Formation of C–C, C–S and C–N bonds catalysed by supported copper nanoparticles
Alexander Yu. Mitrofanov,Arina V. Murashkina,Iris Martín-García,Francisco Alonso,Irina P. Beletskaya Catal. Sci. Technol. 2017 7 4401
3.
Polyfluoroarenes. Part XVII. Some reactions of pentafluorobenzonitrile
J. M. Birchall,R. N. Haszeldine,M. E. Jones J. Chem. Soc. C 1971 1343
4.
SERS-based detection of an organochlorine pesticide through surface plasmon-induced C–C coupling
Douglas S. Lopes,Ester V. Miranda,R?mulo A. Ando,Paola Corio Environ. Sci.: Nano 2023 10 1920
5.
2,3-Functionalization of furans, benzofurans and thiophenes
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Laurin Melzig,Christian B. Rauhut,Paul Knochel via magnesiation and sulfoxide–magnesium exchange. Laurin Melzig Christian B. Rauhut Paul Knochel Chem. Commun. 2009 3536
6.
Trifluoromethylation of (hetero)aryl iodides and bromides with copper(i) chlorodifluoroacetate complexes
Xiaoxi Lin,Zhengyu Li,Xiaoyan Han,Zhiqiang Weng RSC Adv. 2016 6 75465
7.
Ligand-free palladium catalyzed Ullmann biaryl synthesis: ‘household’ reagents and mild reaction conditions
Xinchi Gong,Jie Wu,Yunge Meng,Yulan Zhang,Long-Wu Ye,Chunyin Zhu Green Chem. 2019 21 995
8.
A study of diketopiperazines as electron-donor initiators in transition metal-free haloarene–arene coupling
Florimond Cumine,Shengze Zhou,Tell Tuttle,John A. Murphy Org. Biomol. Chem. 2017 15 3324
9.
Recent advances in synthetic methodologies for transition metal-free Ullmann condensation reactions
Preeti Lalit Pant,Ganapati S. Shankarling New J. Chem. 2018 42 13212
10.
Application of a new kinetic method in the investigation of cleavage reactions of haloaromatic radical anions
Rasmus J. Enem?rke,Torben B. Christensen,Henrik Jensen,Kim Daasbjerg J. Chem. Soc. Perkin Trans. 2 2001 1620
参考资料
Reaxys RN
2041519
Beilstein
9(3)1445
4-碘苯甲腈推荐生产厂家
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联系人:胡灵
QQ:2978041583
上游
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