N-(Z-amino)phthalimide
N-(Z-amino)phthalimide (CAS: 287728-91-0), with the molecular formula C16H12N2O4 and a molecular weight of 296.28 g/mol, is a specialized organic compound. It serves as a valuable building block in chemical synthesis, particularly within the realm of carbonyl compounds and hydrazides. This compound is utilised in research and development settings for the creation of novel molecules and intermediates, contributing to advancements in various chemical fields.
- IUPAC
- N′-Z-N,N-phthaloylhydrazine,N-(Benzyloxycarbonylamino)phthalimide
- Synonyms
- N′-Z-N,N-phthaloylhydrazineN-(Benzyloxycarbonylamino)phthalimide

Organic Synthesis Intermediate
N-(Z-amino)phthalimide is a key intermediate used in the synthesis of more complex organic molecules. Its structure lends itself to various coupling reactions and functional group transformations.
Research and Development
This compound finds application in academic and industrial research laboratories for exploring new synthetic routes and developing novel chemical entities.
Building Block for Heterocycles
As an organic building block, it can be incorporated into the synthesis of diverse heterocyclic compounds, which are prevalent in pharmaceuticals and materials science.
| Molecular weight | 296.28 |
|---|---|
| Empirical formula | C16H12N2O4 |
| Assay | ≥95.0% |
| Melting point | 132-137 °C |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is N-(Z-amino)phthalimide used for?
+
N-(Z-amino)phthalimide is primarily used as a building block and intermediate in organic synthesis and research and development activities.
What are the CAS number and formula for N-(Z-amino)phthalimide?
+
The CAS number for N-(Z-amino)phthalimide is 287728-91-0, and its molecular formula is C16H12N2O4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies N-(Z-amino)phthalimide with an assay of ≥95.0%. We do not represent this product as USP, BP, EP, or any other pharmacopoeia grade.
What are the safety and handling recommendations for N-(Z-amino)phthalimide?
+
Users should wear Eyeshields and Gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. Refer to the Safety Data Sheet for comprehensive handling information.
Is N-(Z-amino)phthalimide a controlled substance?
+
The provided data does not indicate that N-(Z-amino)phthalimide is a controlled substance.
How is N-(Z-amino)phthalimide packed, shipped, and exported?
+
N-(Z-amino)phthalimide is carefully packed to ensure safe transit and is available for export globally by Tech Serve Solutions.
How can I request a sample or quote for N-(Z-amino)phthalimide?
+
To request a sample or a quote, please contact our sales team through the website or by phone.
▶ Related products

3,4,5-Trimethoxybenzylamine
Organic Building Blocks

3,4-dihydroxyphenylacetone
Organic Building Blocks

3-Fluoro-4-methoxybenzonitrile
C8H6FNO
Organic Building Blocks
4-Ethyltoluene
C2H5C6H4CH3
Organic Building Blocks
Fluoroacetic acid
C2H3FO2
Organic Building Blocks
Methoxyacetaldehyde
C3H6O2
Organic Building Blocks
Methyl 4-acetamido-5-chloro-2-methoxybenzoate
Organic Building Blocks

Methyl 5-bromo-2-iodobenzoate
BrC6H3(I)CO2CH3
Organic Building Blocks▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis