19064-69-8

Basic information

• Product Name: 1-AMINOPHTHALAZINE
• Synonyms: 1-AMINOPHTHALAZINE;1-Phthalazinamine;Phthalazin-1-aMine
• CAS NO: 19064-69-8
• Molecular Formula: C₈H₇N₃
• Molecular Weight: 145.16128
• Product Categories: Aromatics Compounds;Aromatics;Amines;Heterocycles
• Mol File: 19064-69-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 213-215°C
• Boiling Point: 423.2 °C at 760 mmHg
• Flash Point: 239.3 °C
• Appearance: /
• Density: 1.292 g/cm³
• Vapor Pressure: 2.28E-07mmHg at 25°C
• Refractive Index: 1.723
• Storage Temp.: -20?C Freezer
• Solubility: DMSO (Sparingly), Methanol (Slightly), Water (Slightly), Nitromethane
• CAS DataBase Reference: 1-AMINOPHTHALAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-AMINOPHTHALAZINE(19064-69-8)
• EPA Substance Registry System: 1-AMINOPHTHALAZINE(19064-69-8)

Safety Data

• Hazardous Substances Data: 19064-69-8(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Solid

InChI:InChI=1/C8H7N3/c9-8-7-4-2-1-3-6(7)5-10-11-8/h1-5H,(H2,9,11)

Upstream product

• 100537-30-2 1-Phenoxy-phthalazin 
• 631-61-8 ammonium acetate 
• 4752-10-7 1,4-dichlorophthalazine 
• 1044569-46-1 1-hydrazinophthalazine 
• 5784-45-2 1-chlorophthalazine 
• 119-39-1 phthalazone 
• 13580-86-4 4-chlorophthalazin-1-ylamine 

Downstream Products

• 101721-36-2 3,4,5-trimethoxy-benzoic acid phthalazin-1-ylamide 
• 108801-20-3 4-nitro-benzenesulfonic acid phthalazin-1-ylamide 
• 132623-76-8 N-acetyl-sulfanilic acid phthalazin-1-ylamide 
• 100962-00-3 N-phthalazin-1-yl-benzamide 
• 304-20-1 hydralazine hydrochloride 
• 109127-95-9 sulfanilic acid phthalazin-1-ylamide 

Relevant articles and documents

PHTHALAZINE DERIVATIVES

Compounds of the formula (I), in which R1, X and n have the meanings indicated in Claim 1, are inhibitors of Tankyrase, and can be employed, inter alia, for the treatment of diseases such as cancer, cardiovascular diseases, central nervous syst

Hydrazination of Pyridazines and Phthalazines

It is shown by 15N-labelling techniques that hydrazination of pyridazines partly occurs according to a reaction pathway, involving addition of the nucleophile (hydrazine), ring opening and ring closure (SN(ANRORC)-mechanism).It is also proved that phthalazines undergo hydrazination without ring opening (SN(AE)-mechanism).