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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Imidazolium, 1-ethyl-3-methyl-, thiocyanate

CC[n+]1ccn(c1)C.[S-]C#N Request for Quotation
Chemical Name: 1H-Imidazolium, 1-ethyl-3-methyl-, thiocyanate
CAS Number: 331717-63-6
Product Number: AG007H5Y(AGN-PC-0O8ZXR)
Synonyms:
MDL No:
Molecular Formula: C7H11N3S
Molecular Weight: 169.2473

Identification/Properties

Computed Properties
Molecular Weight:
169.246g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
169.067g/mol
Monoisotopic Mass:
169.067g/mol
Topological Polar Surface Area:
33.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
104
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Ethyl-3-methylimidazolium thiocyanate, also known as $name$, is a versatile and innovative chemical compound utilized in various chemical synthesis processes. Its unique properties make it a valuable asset in laboratory settings, particularly in organic synthesis and catalysis.This compound serves as an effective catalyst in a wide range of reactions, facilitating the transformation of chemical substances by lowering activation energy barriers. $name$ can be employed in diverse organic transformations, including the synthesis of pharmaceutical intermediates, fine chemicals, and specialty materials.Moreover, 1-Ethyl-3-methylimidazolium thiocyanate demonstrates excellent solubility in a variety of solvents, enabling easy incorporation into reaction mixtures. Its compatibility with different reaction conditions and substrates enhances its utility in complex synthesis pathways, where precise control over reaction parameters is essential for product quality and yield.Overall, the application of 1-Ethyl-3-methylimidazolium thiocyanate in chemical synthesis showcases its significance as a valuable tool for researchers and chemists seeking to streamline their synthetic processes and develop novel compounds with enhanced properties.