N-苯基苄脒 | 1527-91-9
中文名称:
N-苯基苄脒
英文名称:
N-phenylbenzenecarboximidamide
CAS No.:
1527-91-9
分子式:
C1 3 H1 2 N2
分子量:
196.2478
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:N-苯基苄脒结构式
名称和标识符
MDL
MFCD00019730
InChIKey
MPYOKHFSBKUKPQ-UHFFFAOYSA-N
Inchi
1S/C13H12N2/c14-13(11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15)
SMILES
N(/C1C([H])=C([H])C([H])=C([H])C=1[H])=C(\C1C([H])=C([H])C([H])=C([H])C=1[H])/N([H])[H]
BRN
608471
别名信息
- 中文别名 -
N-苯基苄脒
N1-苯基苯-1-羧酰胺
溴化镅
N-苯基苄脒,97%
- 英文别名 -
N-Phenylbenzamidine
N1-Phenylbenzene-1-carboximidamide
N'-phenylbenzenecarboximidamide
N'-Phenylbenzamidine
N-Phenyl-Benzenecarboximidamide
N-phenylbenzimidamide
N-phenyl-benzylamidine
N1-Phenylbenzamidine
N-phenylbenzenecarbimidamide
N-Phenylbenzenecarboximidamide
MPYOKHFSBKUKPQ-UHFFFAOYSA-N
NSC38941
n2-phenylbenzamidine
Maybridge1_004766
(iminophenylmethyl)phenylamine
MLS001005675
Benzenecarboximidamide,N-phenyl-
HMS555A14
Benzenecarboximidamide, N-phenyl-
N-phenylbenzenecarboximidamide
CS-0156575
SCHEMBL24136574
CS-12504
SMR000348939
N-phenylbenzamidine
DTXSID80276781
N-phenyl-benzenecarboximidamide
SCHEMBL139363
SY060407
NCGC00245987-01
EU-0000363
F0345-3709
1527-91-9
MFCD00019730
SCHEMBL24662980
CHEMBL1363621
SR-01000391065
EN300-16689
AE-641/00686063
AKOS001044488
FT-0633637
AKOS024598920
NSC-38941
HMS2720D11
SR-01000391065-1
AC2522
N-Phenylbenzimidamide
N-PHENYLBENZAMIDINE
N1-PHENYLBENZENE-1-CARBOXIMIDAMIDE
物化性质
实验特性
LogP
3.29680
PSA
35.88000
沸点
346.3°C at 760 mmHg
熔点
117 °C
闪点
163.3°C
颜色与性状
粉末。
溶解性
未确定
敏感性
Hygroscopic
密度
1.05
计算特性
精确分子量
196.10000
氢键供体数量
1
氢键受体数量
1
可旋转化学键数量
2
同位素质量
196.1
重原子数量
15
复杂度
211
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)
2.6
互变异构体数量
2
表面电荷
0
拓扑分子极性表面积
38.4
海关数据
海关编码
2925290090
海关数据
中国海关编码:
2925290090
概述:
2925290090 其他亚胺及其衍生物,以及它们的盐。监管条件:无。增值税率:17.0%。退税率:9.0%。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:
2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%
相关文献
1.
88. Diamidides. Part I. Derivatives of triazapentadiene and tetra-azaheptatriene
F. C. Cooper,M. W. Partridge,W. F. Short J. Chem. Soc. 1951 391
2.
43. Diamidides. Part II. 2 : 4-Diaryltriazapentadienes
D. A. Peak J. Chem. Soc. 1952 215
3.
103. Amidines. Part XI. Preparation of amidines by ammonolysis of N-arylamidinium salts
P. Oxley,W. F. Short J. Chem. Soc. 1949 449
4.
52. Preparation of N-substituted amidines
F. C. Cooper,M. W. Partridge J. Chem. Soc. 1953 255
5.
Synthesis and properties of imidazolo-fused benzotriazinyl radicals
Andrey A. Berezin,Christos P. Constantinides,Styliana I. Mirallai,Maria Manoli,Levy L. Cao,Jeremy M. Rawson,Panayiotis A. Koutentis Org. Biomol. Chem. 2013 11 6780
6.
Cobalt-catalyzed intramolecular C–N and C–O cross-coupling reactions: synthesis of benzimidazoles and benzoxazoles
Prasenjit Saha,Md Ashif Ali,Pokhraj Ghosh,Tharmalingam Punniyamurthy Org. Biomol. Chem. 2010 8 5692
7.
430. Cyclic amidines. Part VII. Preparation of benziminazoles from N′-aryl-N-hydroxyamidines
M. W. Partridge,H. A. Turner J. Chem. Soc. 1958 2086
8.
Cyclic amidines. Part I. Derivatives of phenhomazine (dibenzo[b, f]-1 : 5-diazocine)
F. C. Cooper,M. W. Partridge J. Chem. Soc. 1954 3429
9.
Transition metal-catalyzed N-arylations of amidines and guanidines
Tom R. M. Rauws,Bert U. W. Maes Chem. Soc. Rev. 2012 41 2463
10.
N-Benzoylbenzamidinate complexes of aluminium: highly efficient initiators for the ring-opening polymerization of ε-caprolactone
K. Bakthavachalam,Ashwene Rajagopal,N. Dastagiri Reddy Dalton Trans. 2014 43 14816
下游
苯甲腈
溴苯
苯胺,盐酸盐
苯甲脒(盐酸溶液)
苯磺酸铵
硫代苯甲酰胺
N,N'-二亚水杨基-1,3-二氨基丙烷
3,4,5-Triphenyl-4,5-dihydro-1,2,4-oxadiazole
benzenesulphonic acid, compound with aniline (1:1)
N-(α-氯苯亚甲基)苯胺
苯甲亚胺酸乙酯
苯甲醛苯基腙
碘苯
异氰酸4-苄氧基苯酯
N-苯基氰胺
叠氮苯
Benzenemethanamine, a-(2-imino-2-phenylethylidene)-N-phenyl-
3-imino-1,N-diphenyl-2-methyl-3-(4-chlorophenyl)prop-1-enylamine
苯
1,5-二苯基四唑
氨
Benzenemethanamine,a-[2-imino-2-(4-methylphenyl)ethylidene]-N-phenyl-
N-苯甲酰替苯胺
1527-91-9
硝基苯
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