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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)-

5H-Tetrazole-5-thione, 1-[2-(dimethylamino)ethyl]-1,2-dihydro-

CN(CCn1[nH]nnc1=S)C Request for Quotation
Chemical Name: 5H-Tetrazole-5-thione, 1-[2-(dimethylamino)ethyl]-1,2-dihydro-
CAS Number: 61607-68-9
Product Number: AG0032IE(AGN-PC-0KNWO1)
Synonyms:
MDL No: MFCD00082923
Molecular Formula: C5H11N5S
Molecular Weight: 173.2393

Identification/Properties

Properties
MP:
215 °C (dec.)(lit.)
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
173.238g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
173.074g/mol
Monoisotopic Mass:
173.074g/mol
Topological Polar Surface Area:
75.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
178
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-[2-(Dimethylamino)ethyl]-1H-tetrazole-5-thiol, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the field of organic chemistry, particularly in the synthesis of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ is utilized as a thiol-containing reagent to introduce the tetrazole-5-thiol group into organic molecules. The presence of the thiol group allows for various reactions such as thiol-ene click chemistry, thiol-disulfide exchange reactions, and thiol-ene polymerizations. This enables the modification of target molecules with desired functionalities and structural motifs.Moreover, the dimethylaminoethyl moiety in $name$ imparts unique properties to the compound, enhancing its solubility and reactivity in various reaction conditions. This feature makes $name$ a valuable reagent for the synthesis of complex molecules where solubility and reactivity are crucial factors.Overall, the application of 1-[2-(Dimethylamino)ethyl]-1H-tetrazole-5-thiol in chemical synthesis offers a valuable tool for organic chemists to access diverse chemical space, enabling the synthesis of novel compounds with potential applications in pharmaceuticals, materials science, and other fields.