Formula: C9H19NO Molecular weight: IUPAC Standard InChI: InChI=1S/C9H19NO/c1-8(11)7-10-9-5-3-2-4-6-9/h8-11H,2-7H2,1H3 IUPAC Standard InChIKey: HFHPBMVMXFZJNO-UHFFFAOYSA-N CAS Registry Number: 103-00-4 Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Other names: Cyclohexylamine, N-propoxylated; 1-Cyclohexylamino-2-propanol; USAF DO-19; 1-Cyclohexylaminopropan-2-ol Permanent link for this species. Use this link for bookmarking this species for future reference. Information on this page: Notes Other data available: Phase change data Mass spectrum (electron ionization) Options: Switch to calorie-based units Data at NIST subscription sites: NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data) NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage. Notes Go To: Top Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database. Customer support for NIST Standard Reference Data products.
2-(Dimethylamino)-2-methylpropan-1-ol | C6H15NO | CID 23435 - structure, chemical names, physical and chemical properties, classification, patents, literature
1-Methoxy-2-propanol is a methoxy alcohol derivative. The ether being relatively unreactive. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water.
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