1. Home
  2. Carbamimidothioic acid, [(4-chlorophenyl)methyl]-,3-(1H-imidazol-4-yl)propyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Carbamimidothioic acid, [(4-chlorophenyl)methyl]-,3-(1H-imidazol-4-yl)propyl ester

N=C(NCc1ccc(cc1)Cl)SCCCc1cnc[nH]1 Request for Quotation
Chemical Name: Carbamimidothioic acid, [(4-chlorophenyl)methyl]-,3-(1H-imidazol-4-yl)propyl ester
CAS Number: 145231-45-4
Product Number: AG001KP1(AGN-PC-0PWT8P)
Synonyms:
MDL No:
Molecular Formula: C14H17ClN4S
Molecular Weight: 308.8296

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Solubility:
H2O: >20 mg/mL

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The Carbamimidothioic acid, N-[(4-chlorophenyl)methyl]-, 3-(1H-imidazol-5-yl)propyl ester is a versatile compound widely used in chemical synthesis processes, particularly in the production of pharmaceuticals and agrochemicals. This compound serves as a key intermediate in the synthesis of various bioactive molecules due to its unique structure and reactivity.In chemical synthesis, this compound can act as a nucleophile, participating in reactions such as nucleophilic substitution, addition, and condensation reactions. Its functional groups enable it to react with a wide range of other molecules, allowing for the formation of complex structures with specific biological activities.Furthermore, the presence of the imidazole moiety in the structure provides the compound with additional versatility, as imidazoles are known to enhance the biological properties of molecules by interacting with biological receptors and enzymes.Overall, the Carbamimidothioic acid, N-[(4-chlorophenyl)methyl]-, 3-(1H-imidazol-5-yl)propyl ester plays a crucial role in the synthesis of various bioactive compounds, making it a valuable tool for researchers and chemists working in the field of drug development and chemical biology.