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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)-

Lithium 5-methyl-1,3,4-thiadiazole-2-carboxylate

[O-]C(=O)c1nnc(s1)C.[Li+] Request for Quotation
Chemical Name: Lithium 5-methyl-1,3,4-thiadiazole-2-carboxylate
CAS Number: 1810070-07-5
Product Number: AG0022K4(AGN-PC-0WAM8F)
Synonyms:
MDL No:
Molecular Formula: C4H3LiN2O2S
Molecular Weight: 150.0848

Identification/Properties

Computed Properties
Molecular Weight:
150.08g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
150.008g/mol
Monoisotopic Mass:
150.008g/mol
Topological Polar Surface Area:
94.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
134
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Lithium 5-methyl-1,3,4-thiadiazole-2-carboxylate, commonly known as $name$, is a versatile compound often utilized in chemical synthesis due to its unique properties. This compound serves as a critical building block in the creation of various organic molecules, particularly in the development of pharmaceuticals, agrochemicals, and materials science. In chemical synthesis, $name$ acts as a nucleophilic reagent, allowing for efficient and selective reactions with electrophiles to form complex molecular structures. Its incorporation in synthetic routes enables chemists to access novel compounds with potential applications in drug discovery, material design, and other scientific endeavors.