14006-31-6

Basic information

• Product Name: (4-phenyltetrahydro-2H-pyran-4-yl)amine(SALTDATA: HCl)
• Synonyms: (4-phenyltetrahydro-2H-pyran-4-yl)amine(SALTDATA: HCl);Tetrahydro-4-phenyl-2H-pyran-4-aMine;4-phenyloxan-4-amine
• CAS NO: 14006-31-6
• Molecular Formula: C₁₁H₁₅NO
• Molecular Weight: 177.2429
• Mol File: 14006-31-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 284.6±40.0 °C(Predicted)
• Appearance: /
• Density: 1.056±0.06 g/cm3(Predicted)
• PKA: 8.75±0.20(Predicted)
• CAS DataBase Reference: (4-phenyltetrahydro-2H-pyran-4-yl)amine(SALTDATA: HCl)(CAS DataBase Reference)
• NIST Chemistry Reference: (4-phenyltetrahydro-2H-pyran-4-yl)amine(SALTDATA: HCl)(14006-31-6)
• EPA Substance Registry System: (4-phenyltetrahydro-2H-pyran-4-yl)amine(SALTDATA: HCl)(14006-31-6)

Safety Data

• RIDADR: UN2811
• HazardClass: IRRITANT
• Hazardous Substances Data: 14006-31-6(Hazardous Substances Data)

Usage

General Description

"(4-phenyltetrahydro-2H-pyran-4-yl)amine" with SALTDATA: HCl, refers to a chemical compound which is an aminopyran derivative with potential application in chemical and pharmaceutical industries. It is generally seen as a derivative of an amine, which is a chemical species that contains one or more basic nitrogen atoms. The addition of HCl (hydrochloric acid) in the SALTDATA indicates that the compound is expressed as a salt with hydrochloric acid. Salts are ionic compounds that result from the neutralization reaction of an acid and a base. Therefore, "(4-phenyltetrahydro-2H-pyran-4-yl)amine(SALTDATA: HCl)" represents the salt of this amine with hydrochloric acid.

Upstream product

• 1202-81-9 4-phenyltetrahydro-2H-pyran-4-carbonitrile 
• 140-29-4 phenylacetonitrile 
• 939801-34-0 C₁₃H₁₇NO₂ 

Downstream Products

• 939801-35-1 C₂₆H₃₃FN₂O₄ 

Relevant articles and documents

Synthesis method of six-membered ring benzylamine compound

The invention relates to the field of synthesis of organic matters, and particularly discloses a synthesis method of a six-membered ring benzylamine compound, which comprises the following steps: taking a compound D, a compound E and potassium tert-butoxide as raw materials, taking dimethyl sulfoxide as a solvent, reacting at 5-10 DEG C for 1-2 hours, heating to 20 DEG C, reacting, and purifying and separating after the reaction is finished to obtain a compound A; the method comprises the following steps: by taking a compound A, potassium carbonate and hydrogen peroxide as raw materials and dimethyl sulfoxide as a solvent, reacting at 50-65 DEG C, adding ice water to separate out a product after the reaction is finished, filtering and washing to obtain a compound B; dissolving the compound B in acetonitrile, adjusting the pH value to 13-14, adding a saturated sodium hypochlorite solution for reaction, and purifying and washing after the reaction is finished to obtain a compound C; the method has the effect of improving the defect that the synthesis process of the six-membered ring benzylamine compound is not suitable for industrial production.