Synonym: 1,1,4,4-Tetramethyl-1,4-butanediol; 2,5-Dihydroxy-2,5-dimethylhexane; 2,5-Dimethyl-2,5-dihydroxyhexane; 2,5-Dimethyl-2,5-hexanediol; 2,5-Dimethylhexane-2,5-diol
CAS Number: 110-03-2
Empirical Formula (Hill Notation): C8H18O2
Molecular Weight: 146.23
EC Number: 203-731-5
MDL Number: MFCD00004473
Linear Formula: (CH3)2C(OH)CH2CH2C(OH)(CH3)2
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: 143618-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: 143618-500G
| assay |
97% |
| bp |
214-215 °C (lit.) |
| functional group |
hydroxyl |
| InChI |
1S/C8H18O2/c1-7(2,9)5-6-8(3,4)10/h9-10H,5-6H2,1-4H3 |
| InChI key |
ZWNMRZQYWRLGMM-UHFFFAOYSA-N |
| mp |
86-90 °C (lit.) |
| Quality Level |
100  |
| SMILES string |
CC(C)(O)CCC(C)(C)O |
| Application: |
2,5-Dimethyl-2,5-hexanediol was used in the synthesis of six- and seven-membered heterocyclic boron compounds containing intramolecular N-B bond. |
| General description: |
2,5-Dimethyl-2,5-hexanediol on heteropoly acid catalyzed dehydration yields cyclic ethers via stereospecific intramolecular SN2 mechanism. It reacts with nitriles in concentrated sulfuric acid to yield Δ1-pyrrolines. |
| Packaging: |
100, 500 g in poly bottle |
| Purity |
97% |
| bp |
214-215 °C (lit.) |
| mp |
86-90 °C (lit.) |
| UNSPSC |
12352100 |
