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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)-

Methanimidic acid, 1-methylethyl ester, hydrochloride

N=COC(C)C.Cl Request for Quotation
Chemical Name: Methanimidic acid, 1-methylethyl ester, hydrochloride
CAS Number: 16694-44-3
Product Number: AG001X0C(AGN-PC-0NKCFV)
Synonyms:
MDL No:
Molecular Formula: C4H10ClNO
Molecular Weight: 123.5813

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Chemical Structure


Isopropyl formimidate hydrochloride is a versatile chemical compound commonly used in chemical synthesis processes. It serves as a key reagent in various reactions, particularly in the formation of amides and carbamates. With its ability to readily react with various nucleophiles, Isopropyl formimidate hydrochloride plays a crucial role in the efficient synthesis of complex organic molecules. Its compatibility with a wide range of functional groups and its high reactivity make it a valuable tool for chemists working in the field of organic synthesis. Additionally, Isopropyl formimidate hydrochloride offers the advantage of being easily handled and stored, making it a popular choice for researchers and industrial chemists alike.