900799-69-1

Basic information

• Product Name: 3-Amino-5-hydroxybenzoic acid, N-CBZ protected
• Synonyms: 3-{[(Benzyloxy)carbonyl]amino}-5-hydroxybenzoic acid;3-Amino-5-hydroxybenzoic acid, N-CBZ protected;3-Amino-5-hydroxybenzoic acid, N-CBZ protected 97%;N-CBZ-3-AMINO-5-HYDROXYBENZOIC ACID;3-(Cbz-aMino)-5-hydroxybenzoic Acid;3-(N-Cbz-aMino)-5-hydroxybenzoic Acid;3-Amino-5-hydroxybenzoicacid,N-CBZprotected97%
• CAS NO: 900799-69-1
• Molecular Formula: C₁₅H₁₃NO₅
• Molecular Weight: 287.26742
• Mol File: 900799-69-1.mol

Chemical Properties

• Melting Point: 216-220.5
• Boiling Point: 486.2°C at 760 mmHg
• Flash Point: 247.8°C
• Appearance: /
• Density: 1.432g/cm³
• Vapor Pressure: 2.9E-10mmHg at 25°C
• Refractive Index: 1.677
• CAS DataBase Reference: 3-Amino-5-hydroxybenzoic acid, N-CBZ protected(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Amino-5-hydroxybenzoic acid, N-CBZ protected(900799-69-1)
• EPA Substance Registry System: 3-Amino-5-hydroxybenzoic acid, N-CBZ protected(900799-69-1)

Safety Data

• Hazardous Substances Data: 900799-69-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-Amino-5-hydroxybenzoic acid, N-CBZ protected, is used as a key intermediate for the synthesis of various pharmaceuticals. Its protected amine group allows for selective reactions, facilitating the development of complex drug molecules with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Amino-5-hydroxybenzoic acid, N-CBZ protected, serves as an essential building block for the synthesis of agrochemicals. Its versatility and reactivity contribute to the creation of effective compounds for crop protection and other agricultural applications.
Used in Organic Synthesis:
3-Amino-5-hydroxybenzoic acid, N-CBZ protected, is utilized as a valuable building block in organic synthesis. Its unique structure and reactivity enable the synthesis of complex organic molecules, making it an indispensable component in the development of new chemical products and materials.
Used in Research and Development:
In research and development, 3-Amino-5-hydroxybenzoic acid, N-CBZ protected, is employed as a versatile tool for exploring new chemical reactions and developing innovative synthetic routes. Its protected amine group allows for selective reactions, providing researchers with the flexibility to investigate various chemical transformations and optimize reaction conditions.

InChI:InChI=1/C15H13NO5/c17-13-7-11(14(18)19)6-12(8-13)16-15(20)21-9-10-4-2-1-3-5-10/h1-8,17H,9H2,(H,16,20)(H,18,19)

Upstream product

• 76045-71-1 3-amino-5-hydroxybenzoic acid 
• 501-53-1 benzyl chloroformate 

Relevant articles and documents

Macrocyclic Compounds Useful as Bace Inhibitors

The invention relates to novel macrocyclic compounds of the formula (I), in which all of the variables are as defined in the specification, the number of ring atoms included in the macrocyclic ring being 14, 15, 16 or 17, in free base form or in acid addition salt form, to their preparation, to their use as medicaments and to medicaments comprising them.