27697-51-4 ((Ethanaminium,N,N,N-trimethyl-, chloride (1:1))

快速询单

结构式：

Ethanaminium,N,N,N-trimethyl-, chloride (1:1)MOL文件

CAS号：

27697-51-4

英文名称：

Ethanaminium,N,N,N-trimethyl-, chloride (1:1)

分子式：

C₅H₁₄ClN

分子量：

123.624360561371

Ethanaminium,N,N,N-trimethyl-, chloride (1:1)(27697-51-4)名称与标识符

名称

英文别名：

Ethanaminium,N,N,N-trimethyl-, chloride (1:1);Ethyltrimethylaminium·chloride;ethyltrimethylammonium chloride;Ammonium,ethyltrimethyl-, chloride (8CI);Ethanaminium, N,N,N-trimethyl-, chloride(9CI);Ethyltrimethylammonium chloride (6CI);Trimethylethylammonium chloride;Ethanaminium, N,N,N-trimethyl-, chloride;SCHEMBL370134;ethyl(trimethyl)azanium;chloride;Ethyltrimethylaminium.chloride;DTXSID40885398;Ethanaminium, N,N,N-trimethyl-, chloride (1:1);N,N,N-TRIMETHYLETHANAMINIUMCHLORIDE;UXYBXUYUKHUNOM-UHFFFAOYSA-M;ethyl trimethyl ammonium chloride;27697-51-4;N,N,N-TRIMETHYLETHANAMINIUM CHLORIDE;

标识符

InChIKey：

UXYBXUYUKHUNOM-UHFFFAOYSA-M

Inchi：

1S/C5H14N.ClH/c1-5-6(2,3)4;/h5H2,1-4H3;1H/q+1;/p-1

SMILES：

[Cl-].[N+](C)(C)(C)CC

Ethanaminium,N,N,N-trimethyl-, chloride (1:1)(27697-51-4)物化性质

计算特性

精确分子量 : 123.0814771g/mol
氢键供体数量 : 0
氢键受体数量 : 1
可旋转化学键数量 : 1
同位素质量 : 123.0814771g/mol
重原子数量 : 7
复杂度 : 33.7
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 : 2
拓扑分子极性表面积 : 0Å²

Ethanaminium,N,N,N-trimethyl-, chloride (1:1)(27697-51-4)推荐厂家更多厂家(1)

公司名称	手机号/电话	联系人	QQ	微信	询单
JACS-郑州杰克斯化工产品有限公司	15981966935 0371-86259281	杰克斯JACS	893596907		询单

Ethanaminium,N,N,N-trimethyl-, chloride (1:1)(27697-51-4)相关文献

1. Evaluation of toxicity and biodegradability for cholinium-based deep eutectic solvents
Ibrahim Juneidi,Maan Hayyan,Mohd Ali Hashim RSC Adv. 2015 5 83636
2. Reline aqueous solutions behaving as liquid mixtures of H-bonded co-solvents: microphase segregation and formation of co-continuous structures as indicated by Brillouin and 1H NMR spectroscopies
E. Posada,N. López-Salas,R. J. Jiménez Riobóo,M. L. Ferrer,M. C. Gutiérrez,F. del Monte Phys. Chem. Chem. Phys. 2017 19 17103
3. The separation and determination of rhodium and iridium
E. Jackson Analyst 1959 84 106
4. Stereoselectivity of epoxidation of substituted cyclohexa-1,4-dienes: influence of an allylic methoxycarbonyl group
Talat Mah,Hasnah M. Sirat,Eric J. Thomas J. Chem. Soc. Perkin Trans. 1 1979 2255
5. CCCXLIX.—The relative directive powers of groups of the forms RO and RR′N in aromatic substitution. Part VIII. The nitration of 4-n-butoxyanisole
John Clarke,Robert Robinson,John Charles Smith J. Chem. Soc. 1927 2647
6. Cyclization of substituted 2′-hydroxychalcones to flavanones. Solvent and isotope effects
Jorge J. P. Furlong,N. Sbarbati Nudelman J. Chem. Soc. Perkin Trans. 2 1988 1213
7. Mineralogical chemistry
J. Chem. Soc. Abstr. 1878 34 940
8. Dioxygenase-catalysed oxidation of monosubstituted thiophenes: sulfoxidation versus dihydrodiol formation
Derek R. Boyd,Narain D. Sharma,Nimal Gunaratne,Simon A. Haughey,Martina A. Kennedy,John F. Malone,Christopher C. R. Allen,Howard Dalton Org. Biomol. Chem. 2003 1 984
9. Notes
G. M. Badger,P. Cheuychit,W. H. F. Sasse,T. C. W. Mak,J. Trotter,A. R. Battersby,D. J. Le Count,W. P. Griffith,Z. S. Krzeminski,S. J. Angyal,B. H. M. Billinge,B. G. Gowenlock,G. M. Brooke,J. Burdon,J. C. Tatlow,S. J. Gregg,R. F. S. Tyson,W. Carruthers,J. R. Plimmer,D. Lavie,Y. Shvo,O. R. Gottlieb,R. B. Desai,M. L. Khorana,A. Holland,Leo A. Pohoryles,Izhar Gat,Shalom Sarel,J. D. Loudon,A. D. B. Sloan,Peter Bladon,Thomas Sleigh,W. Hewertson,R. A. Shaw,B. C. Smith,J. Chatt,B. L. Shaw,A. A. Williams,M. Halmann,L. Kugel,G. W. Kirby,G. Shaw,A. Yeadon,H. J. Emeléus,G. L. Hurst,John G. Carey,Ian T. Millar,Stanley S. Brown,Roy Wade,D. H. Brown,D. J. Alner J. Chem. Soc. 1962 3241

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