CAS 16156-55-1
:1-Butanol, 3-methyl-, 1-methanesulfonate
Description:
1-Butanol, 3-methyl-, 1-methanesulfonate, also known by its CAS number 16156-55-1, is an organic compound characterized by its structure, which includes a butanol backbone with a methyl group at the third carbon and a methanesulfonate functional group. This compound is typically a colorless to pale yellow liquid and is soluble in polar solvents due to the presence of the sulfonate group, which enhances its hydrophilicity. It exhibits properties typical of alcohols, such as the ability to participate in hydrogen bonding, which can influence its boiling point and reactivity. The methanesulfonate group can act as a leaving group in nucleophilic substitution reactions, making this compound useful in various synthetic applications. Additionally, it may have applications in the fields of pharmaceuticals, agrochemicals, and as a reagent in organic synthesis. Safety data indicates that, like many organic solvents, it should be handled with care, as it may pose health risks upon exposure.
Formula:C6H14O3S
InChI:InChI=1S/C6H14O3S/c1-6(2)4-5-9-10(3,7)8/h6H,4-5H2,1-3H3
InChI key:InChIKey=CPKOUXPEJOKKNM-UHFFFAOYSA-N
SMILES:O(CCC(C)C)S(C)(=O)=O
Synonyms:- 1-Butanol, 3-methyl-, 1-methanesulfonate
- 1-Butanol, 3-methyl-, methanesulfonate
- 3-Methylbutyl Methanesulfonate
- Ccris 9157
- Isopentyl alcohol, methanesulfonate
- Isopentyl methanesulfonate
- Methanesulfonic acid 3-methylbutyl ester
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Found 3 products.
Isopentyl Mesylate
CAS:Controlled Product<p>Stability Moisture Sensitive<br>Applications Isopentyl Mesylate is used as a reagent in the synthesis of phosphonate derivatives as autotaxin (ATX) inhibitors.<br>References Cui, P., et al.: Bioorg. Med. Chem. Lett., 17, 1634 (2007)<br></p>Formula:C6H14O3SColor and Shape:NeatMolecular weight:166.24
