1. Home
  2. 1H-Isoindol-4-amine, 2,3-dihydro-

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)-

1H-Isoindol-4-amine, 2,3-dihydro-

Nc1cccc2c1CNC2 Request for Quotation
Chemical Name: 1H-Isoindol-4-amine, 2,3-dihydro-
CAS Number: 92203-86-6
Product Number: AG00IH1T(AGN-PC-002KUE)
Synonyms:
MDL No:
Molecular Formula: C8H10N2
Molecular Weight: 134.1784

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

Request for Quotation

Customer Feedback

Chemical Structure


Isoindolin-4-amine is a versatile compound commonly employed in chemical synthesis for its reactivity and ability to participate in various reactions. It serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and advanced materials. In organic synthesis, Isoindolin-4-amine is frequently used as a key intermediate in the creation of complex molecular structures. Its unique molecular structure and functional groups make it a valuable tool for creating diverse compounds with different properties and applications. As a result, Isoindolin-4-amine plays a crucial role in the development of new and innovative chemical products.