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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)-

Hydrazine, hydrochloride

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Chemical Name: Hydrazine, hydrochloride
CAS Number: 14011-37-1
Product Number: AG00AHZY(AGN-PC-0JLJV3)
Synonyms:
MDL No:
Molecular Formula: ClH5N2
Molecular Weight: 68.5061

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Chemical Structure


Hydrazine hydrochloride is a versatile chemical compound commonly used in chemical synthesis for a variety of applications. As a powerful reducing agent, it is often employed in organic chemistry reactions to facilitate the conversion of functional groups or to produce specific products. Additionally, hydrazine hydrochloride is utilized in the synthesis of pharmaceuticals, agricultural chemicals, and specialty chemicals due to its ability to react with various compounds in a controlled manner. Its unique properties make it an essential reagent in the field of organic synthesis, where precise control over reactions and high purity products are crucial. By leveraging the reactivity of hydrazine hydrochloride, chemists can efficiently design and produce a wide range of compounds with tailored properties, making it a valuable tool in modern chemical research and development.