108262-66-4

Basic information

• Product Name: 5-AMino-2-Methyl-2-pentanol
• Synonyms: 5-AMino-2-Methyl-2-pentanol
• CAS NO: 108262-66-4
• Molecular Formula: C₆H₁₅NO
• Molecular Weight: 117.1894
• Mol File: 108262-66-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 5-AMino-2-Methyl-2-pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-AMino-2-Methyl-2-pentanol(108262-66-4)
• EPA Substance Registry System: 5-AMino-2-Methyl-2-pentanol(108262-66-4)

Safety Data

• Hazardous Substances Data: 108262-66-4(Hazardous Substances Data)

Usage

General Description

5-Amino-2-methyl-2-pentanol is a chemical compound with the molecular formula C6H15NO. It is a tertiary amine and an alcohol, and is commonly used as a reagent in organic synthesis. 5-AMino-2-Methyl-2-pentanol may also be used in the production of pharmaceuticals, pesticides, and other chemical products. It is an important intermediate in the synthesis of various organic compounds, and its versatile chemical properties make it a valuable building block in the development of new products and materials. Additionally, 5-amino-2-methyl-2-pentanol has potential industrial applications as a corrosion inhibitor and a surfactant due to its unique chemical structure.

Upstream product

• 5344-20-7 4-methyl pentanamine 
• 1455037-19-0 5-(dibenzylamino)-2-methylpentan-2-ol 
• 1305317-96-7 3,7-dimethyl-1-(4-metylpentyl)-1H-purine-2,6-(2H,6H)-dione 
• 107767-68-0 1-(4-Hydroxy-4-methylpentyl)-3,7-dimethyl-1H-purine-2,6(3H,7H)-dione 

Downstream Products

• 123296-19-5 N-(3-hydroxy-4-methylpentyl)benzamide 

Relevant articles and documents

Remote C(sp3)-H Oxygenation of Protonated Aliphatic Amines with Potassium Persulfate

This letter describes the development of a method for selective remote C(sp3)-H oxygenation of protonated aliphatic amines using aqueous potassium persulfate. Protonation serves to deactivate the proximal C(sp3)-H bonds of the amine substrates and also renders the amines soluble in the aqueous medium. These reactions proceed under relatively mild conditions (within 2 h at 80 °C with amine as limiting reagent) and do not require a transition metal catalyst. This method is applicable to a variety of types of C(sp3)-H bonds, including 3°, 2°, and benzylic C-H sites in primary, secondary, and tertiary amine substrates.

Novel indazoles for the treatment and prophylaxis of respiratory syncytial virus infection

The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5, R7, A1, A2 and A3 are as described herein, compositions including the compounds and methods of using the compounds.

Predictable stereoselective and chemoselective hydroxylations and epoxidations with P450 3A4

Enantioselective hydroxylation of one specific methylene in the presence of many similar groups is debatably the most challenging chemical transformation. Although chemists have recently made progress toward the hydroxylation of inactivated C-H bonds, enzymes such as P450s (CYPs) remain unsurpassed in specificity and scope. The substrate promiscuity of many P450s is desirable for synthetic applications; however, the inability to predict the products of these enzymatic reactions is impeding advancement. We demonstrate here the utility of a chemical auxiliary to control the selectivity of CYP3A4 reactions. When linked to substrates, inexpensive, achiral theobromine directs the reaction to produce hydroxylation or epoxidation at the fourth carbon from the auxiliary with pro-R facial selectivity. This strategy provides a versatile yet controllable system for regio-, chemo-, and stereoselective oxidations at inactivated C-H bonds and demonstrates the utility of chemical auxiliaries to mediate the activity of highly promiscuous enzymes.