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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, (3,5-dimethoxyphenyl)-

NNc1cc(OC)cc(c1)OC Request for Quotation
Chemical Name: Hydrazine, (3,5-dimethoxyphenyl)-
CAS Number: 96406-93-8
Product Number: AG0067R5(AGN-PC-0NKINY)
Synonyms:
MDL No:
Molecular Formula: C8H12N2O2
Molecular Weight: 168.1931

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (3,5-Dimethoxyphenyl)hydrazine in chemical synthesis is primarily seen in the field of organic chemistry. This compound, known for its hydrazine functional group and substituted phenyl ring, serves as a versatile building block in the creation of various organic molecules. In chemical synthesis, (3,5-Dimethoxyphenyl)hydrazine can undergo transformations such as nucleophilic substitution, condensation reactions, and oxidation processes to facilitate the formation of new compounds. Its reactivity allows for the introduction of the (3,5-dimethoxyphenyl)hydrazine moiety into complex molecular structures, enabling the synthesis of pharmaceuticals, agrochemicals, and functionalized materials. By participating in reactions with different functional groups, (3,5-Dimethoxyphenyl)hydrazine can act as a key intermediate in the preparation of diverse organic compounds with tailored properties and applications. Its versatility and synthetic utility make it a valuable tool for chemists engaged in the design and production of novel molecular entities.