112225-62-4

Basic information

• Product Name: (2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl)
• Synonyms: (2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl);(2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine;(2,2,6-trimethylchroman-4-yl)amine;2,2,6-trimethyl-4-chromanamine;2,2,6-trimethylchroman-4-amine;MFCD09262260
• CAS NO: 112225-62-4
• Molecular Formula: C12H17NO
• Molecular Weight: 191.26948
• Mol File: 112225-62-4.mol

Chemical Properties

• Boiling Point: 268.8±39.0 °C(Predicted)
• Appearance: /
• Density: 1.008±0.06 g/cm3(Predicted)
• PKA: 8.87±0.40(Predicted)
• CAS DataBase Reference: (2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl)(CAS DataBase Reference)
• NIST Chemistry Reference: (2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl)(112225-62-4)
• EPA Substance Registry System: (2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl)(112225-62-4)

Safety Data

• Hazardous Substances Data: 112225-62-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Drug Formulation:
(2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl) is used as a building block in the formulation of pharmaceutical compounds. Its crystalline powder form and solubility properties contribute to the stability and effectiveness of drug formulations.
Used in Research and Development:
(2,2,6-trimethyl-3,4-dihydro-2H-chromen-4-yl)amine(SALTDATA: HCl) is used as a valuable tool in pharmaceutical research and development. Its versatility and importance in the synthesis of new medications make it a key component in the creation of innovative treatments for various medical conditions.

Upstream product

• 63678-14-8 2,2,6-trimethyl-4-chromanone 

Relevant articles and documents

Asymmetric synthesis of 4-amino-3,4-dihydro-2,2-dimethyl-2H-1 benzopyrans

Highly enantioselactive reduction of 3,4-dihydro-2,2-dimethyl-2H-1- benzopyran-4-ones 3 a-e by BH3 was achieved in the presence of catalytic amounts of Corey's oxazaborolidine 4 to afford the corresponding 3,4-dihydro- 2,2-dimethyl-2H-1-benzopy

Sulfonamide-substituted chromans, processes for their preparation, their use as a medicament or diagnostic, and pharmaceutical preparations comprising them

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