2-(氯甲基)萘 | 2506-41-4
中文名称：
2-(氯甲基)萘
英文名称：
2-(chloromethyl)naphthalene
CAS No.：
2506-41-4
分子式：
C1 1 H9 Cl
分子量：
176.64216
名称和标识符
MDL
MFCD00046488
InChIKey
MPCHQYWZAVTABQ-UHFFFAOYSA-N
Inchi
InChI=1S/C11H9Cl/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2
SMILES
C1=CC=C2C=C(C=CC2=C1)CCl
别名信息
- 中文别名 -
2-(氯甲基)萘
2-氯甲基奈
2-氯甲基萘
Β-(氯甲基)萘
- 英文别名 -
2-(chloromethyl)naphthalene
1-(chloromethyl)-naphthalene
2-(3-METHOXY-PHENYL)-7-METHYL-3-PIPERAZIN-1
2-(chloroethyl)naphthalene
2-(chloromethyl)naphtalene
2-(chloromethyl)-naphthalene
2-naphthylmethyl chloride
2-Menaphthyl chloride
NSC 408896
Naphthalen-2-ylmethyl chloride
beta-Chloromethylnaphthalene
beta-Naphthylmethyl chloride
2-Naphthylmethyl chloride
NSC408896
XMM44Z9B62
NS00027799
naphthalen-2-ylmethyl chloride
NSC-408896
DTXSID30179753
BS-16256
2-Phenyl-2-(2-Piperidine)Acetamide
W-107265
FT-0634332
2-(chloromethyl) naphthalene
SCHEMBL905392
2-chloromethyl-naphthalene
F3395-0168
AKOS000261866
MPCHQYWZAVTABQ-UHFFFAOYSA-N
UNII-XMM44Z9B62
3-chloro-methylnaphthalene
2-(Chloromethyl)naphthalene, >=97.0%
EINECS 219-713-5
beta-chloromethylnaphthalene
MFCD00046488
2-chloromethyl naphthalene
beta-chloromethylnapthalene
Naphthalene, 2-(chloromethyl)-
2506-41-4
2-(Chloromethyl)naphthalene
2-Chloromethylnaphthalene
物化性质
实验特性
LogP
3.57860
PSA
0.00000
折射率
1.6323 (estimate)
沸点
168 ºC (20 Torr)
熔点
48.5 ºC
闪点
129.9±11.4 ºC,
溶解度
Insuluble (4.4E-3 g/L) (25 ºC),
颜色与性状
茶色颗粒
溶解性
溶于苯、乙醇。
敏感性
对湿度敏感
密度
1.167±0.06 g/cm3 (20 ºC 760 Torr),
计算特性
精确分子量
176.03900
氢键供体数量
0
氢键受体数量
0
可旋转化学键数量
1
同位素质量
176.039
重原子数量
12
复杂度
144
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
0A^2
相关文献
1.
Nanohybrid materials from the intercalation of imidazolium ionic liquids in kaolinite Sadok Letaief,Christian Detellier J. Mater. Chem. 2007 17 1476
2.
Synthesis of trans-stilbenes via phosphine-catalyzed coupling reactions of benzylic halides Sheng Zhang,Zhilong Xie,Zhanqiang Ye,Mingyang Zhang,Dongdeng Li,Masahiko Yamaguchi,Ming Bao Org. Biomol. Chem. 2022 20 6869
3.
Selective aerobic oxidation of halides and amines with an inorganic-ligand supported zinc catalyst
Jingjing Wang,Yongyan Zhai,Ying Wang,Han Yu,Wenshu Zhao,Yongge Wei Dalton Trans. 2018 47 13323
4.
An efficient transformation of primary halides into nitriles through palladium-catalyzed hydrogen transfer reaction
Tao Zou,Xiaoqiang Yu,Xiujuan Feng,Ming Bao Chem. Commun. 2015 51 10714
5.
Well-defined N-heterocyclic carbene silver halides of 1-cyclohexyl-3-arylmethylimidazolylidenes: synthesis, structure and catalysis in A3-reaction of aldehydes, amines and alkynes
Yanbo Li,Xiaofeng Chen,Yin Song,Ling Fang,Gang Zou Dalton Trans. 2011 40 2046
6.
An efficient protocol for the preparation of aldehydes/ketones and imines by an inorganic-ligand supported iron catalyst
Yongyan Zhai,Mengqi Zhang,Haibin Fang,Shi Ru,Han Yu,Wenshu Zhao,Yongge Wei Org. Chem. Front. 2018 5 3454
7.
Recent progress on the construction of axial chirality through transition-metal-catalyzed benzannulation
Qian Zhao,Cheng Peng,Yu-Ting Wang,Gu Zhan,Bo Han Org. Chem. Front. 2021 8 2772
8.
Direct palladium-catalyzed alkenylation, benzylation and alkylation of ethyl oxazole-4-carboxylate with alkenyl-, benzyl- and alkyl halides
Cécile Verrier,Christophe Hoarau,Francis Marsais Org. Biomol. Chem. 2009 7 647
9.
Synthesis of mixed phosphorotrithioates from white phosphorus
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10.
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