13439-98-0 Usage
General Description
3-methyl-1,1-bis(2-methylpropoxy)butane is a chemical compound with the molecular formula C13H28O2. It is also known by its IUPAC name, 3,3-bis(2-methylpropoxy)hexane. 3-methyl-1,1-bis(2-methylpropoxy)butane is a colorless, flammable liquid that is insoluble in water. It is commonly used as a solvent and in the production of other chemicals. It is important to handle this compound with care, as it can be harmful if swallowed, inhaled, or absorbed through the skin. It may also cause irritation to the eyes and respiratory system. 3-methyl-1,1-bis(2-methylpropoxy)butane should be stored in a cool, well-ventilated area away from sources of ignition and incompatible materials.
Check Digit Verification of cas no
The CAS Registry Mumber 13439-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13439-98:
(7*1)+(6*3)+(5*4)+(4*3)+(3*9)+(2*9)+(1*8)=110
110 % 10 = 0
So 13439-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H28O2/c1-10(2)7-13(14-8-11(3)4)15-9-12(5)6/h10-13H,7-9H2,1-6H3
13439-98-0Relevant articles and documents
VARIATIONS ON PRINS-LIKE CHEMISTRY TO PRODUCE 2,5-DIMETHYLHEXADIENE FROM ISOBUTANOL
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Page/Page column 6, (2012/11/07)
The method of the present invention provides a high yield pathway to 2,5-dimethylhexadiene from renewable isobutanol, which enables economic production of renewable p-xylene (and subsequently, terephthalic acid, a key monomer in the production of PET) from isobutanol. In addition, the present invention provides methods for producing 2,5-dimethylhexadiene from a variety of feed stocks that can act as “equivalents” of isobutylene and/or isobutyraldehyde including isobutanol, isobutylene oxide, and isobutyl ethers and acetals. Catalysts employed in the present methods that produce 2,5-dimethylhexadiene can also catalyze alcohol dehydration, alcohol oxidation, epoxide rearrangement, and ether and acetal cleavage.
