CAS 3468-11-9

1-Imino-1H-isoindol-3-amine

Description:

1-Imino-1H-isoindol-3-amine, with the CAS number 3468-11-9, is a chemical compound characterized by its unique structure, which includes an isoindole framework. This compound features an imino group (-NH) and an amino group (-NH2) attached to the isoindole ring, contributing to its reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit properties such as solubility in polar solvents, depending on the specific conditions. The presence of both imino and amino functional groups suggests that it could participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. This compound may also have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural similarity to biologically active molecules. However, detailed studies on its specific properties, reactivity, and potential applications are necessary to fully understand its behavior in different chemical environments.

Formula: C₈H₇N₃

InChI: InChI=1S/C8H7N3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4H,(H3,9,10,11)

InChI key: InChIKey=RZVCEPSDYHAHLX-UHFFFAOYSA-N

SMILES: NC=1C=2C(C(=N)N1)=CC=CC2

Synonyms:

• (1Z)-1-imino-1H-isoindol-3-amine
• 1,3-Diiminoisoindolenine
• 1,3-Diiminoisoindolin
• 1,3-Diiminoisoindolin [Czech]
• 1-Amino-3-iminoisoindolenine
• 1-Imino-1H-isoindol-3-amine
• 1H-Isoindol-3-amine, 1-imino-
• 1H-Isoindole, 3-amino-1-imino-
• 2,3-Dihydro-1H-isoindole-1,3-diimine
• 3-Amino-1-imino-1H-isoindole
• 3-Amino-1H-isoindol-1-imine
• 3-Iminoisoindol-1-amine
• 3-Iminoisoindolenin-1-amine
• Afastogen Blue 5040
• Aminoiminoisoindolenine
• Bis(diiminoisoindoline)
• Diiminoisoindoline
• Fastogen Blue 5040
• Fastogen Blue FP-3100
• Fastogen Blue SH-100
• Isoindoline, 1,3-diimino-
• Modr Ftalostanova 3G [Czech]
• Modr ftalostanova 3g
• Nsc 516222
• Phthalimidimide
• Phthalocyanine Blue 01206
• Phthalocyanine Blue 01216

1,3-Diiminoisoindoline

CAS: 3468-11-9, 57500-34-2

Formula: C₈H₇N₃

Purity: >98.0%(T)

Color and Shape: Light yellow to Yellow to Green powder to crystal

Molecular weight: 145.17

Ref: 3B-D2079

1,3-Diiminoisoindoline

CAS: 3468-11-9

Formula: C₈H₇N₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 145.1613

Ref: IN-DA00BXFJ

1,3-Diiminoisoindoline

CAS: 3468-11-9

Formula: C₈H₇N₃

Molecular weight: 145.16

Ref: 7W-GT5882

1-Imino-1H-Isoindol-3-Amine

CAS: 3468-11-9

1-Imino-1H-Isoindol-3-Amine

Purity: 98%

Molecular weight: 145.16g/mol

Ref: 54-OR1026783

1,3-Diiminoisoindoline

Controlled Product

CAS: 3468-11-9

Applications 1,3-Diiminoisoindoline is a useful compound in the production of colouring compositions. Dyes and metabolites.
References Matsumoto, T., et al.: PCT Int. Appl. (2020), WO 2020218262 A1

Formula: C₈H₇N₃

Color and Shape: Light Yellow

Molecular weight: 145.17

Ref: TR-D455198

Isoindoline-1,3-diimine

CAS: 3468-11-9

Formula: C₈H₇N₃

Purity: 98%

Color and Shape: Crystalline Powder

Molecular weight: 145.165

Ref: 10-F243129

1,3-Diiminoisoindoline

CAS: 3468-11-9

N-Dimethylformamide is a solvent that has been extensively used in the synthesis of dyes and pharmaceuticals. 1,3-Diiminoisoindoline is a copper complex that is formed by reacting N-dimethylformamide with copper(II) chloride or copper(I) iodide. It has been shown to have photochemical properties and can be used as an anticancer drug. The isolated yield of 1,3-diiminoisoindoline can be increased by using palladium complexes or nitrogen atoms in its structure. This compound also reacts with hydrochloric acid to form hydrogen chloride gas and diiminoisoindoline. The hydrogen bonds between these two molecules are crucial for this reaction to occur.

Formula: C₈H₇N₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 145.16 g/mol

Ref: 3D-FD30335