13439-98-0 Usage
Uses
Used in Chemical Industry:
3-methyl-1,1-bis(2-methylpropoxy)butane is used as a solvent for various applications in the chemical industry, due to its ability to dissolve a wide range of substances.
Used in Production of Other Chemicals:
It serves as an intermediate in the synthesis of other chemical compounds, contributing to the versatility and utility of chemical manufacturing processes.
Safety and Storage:
3-methyl-1,1-bis(2-methylpropoxy)butane should be stored in a cool, well-ventilated area to mitigate the risk of fire or explosion, and kept away from sources of ignition and incompatible materials to ensure safe handling and storage conditions.
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 academic research and scientific papers
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.
