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What is phenol 2 propanol used for?
2-Phenyl-2-propanol, 98+%, Thermo Scientific™ It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is used as chemical intermediate. Insoluble in water.
What is the structure of 1 phenyl propan 2 ol?
1-Phenyl-2-propanol
| PubChem CID | 94185 |
|---|---|
| Structure | Find Similar Structures |
| Molecular Formula | C9H12O |
| Synonyms | 1-Phenyl-2-propanol 1-Phenylpropan-2-ol 698-87-3 14898-87-4 Benzyl methyl carbinol More… |
| Molecular Weight | 136.19 |
Is 2 phenyl 1 propanol primary or tertiary?
2-Phenyl-2-propanol is a member of the fragrance structural group Aryl Alkyl Alcohols and is a tertiary alcohol.
Is 2-phenyl-2-propanol a tertiary alcohol?
2-PHENYL-2-PROPANOL Chemical Properties,Uses,Production ChEBI: A tertiary alcohol that is isopropanol in which the hydrogen attached to the carbon bearing the hydroxy group has been replaced by a phenyl group.
What is structure of phenyl?
Phenyl groups have six carbon atoms bonded together in a hexagonal planar ring, five of which are bonded to individual hydrogen atoms, with the remaining carbon bonded to a substituent. Phenyl groups are commonplace in organic chemistry.
What is the structure of 3 Cyclohexylpentan 3 OL?
3-cyclohexylpentan-3-ol
| Compound number: | MolPort-011-893-521 |
|---|---|
| IUPAC traditional: | 3-cyclohexylpentan-3-ol |
| SMILES: | CCC(O)(CC)C1CCCCC1 |
| InChI key: | CJXIUXXPIYXGCT-UHFFFAOYSA-N |
| Molecular formula: | C11H22O |
What is the melting point of 1 phenyl 1 propanol?
3D Structure for HMDB0031627 (1-Phenyl-1-propanol)
| Property | Value |
|---|---|
| Melting Point | Not Available |
| Boiling Point | 103.00 °C. @ 14.00 mm Hg |
| Water Solubility | 0.6 g/L @ 20 °C (exp) |
| LogP | 1.919 (est) |
Which alcohol is known as wood alcohol?
methanol
methanol (CH3OH), also called methyl alcohol, wood alcohol, or wood spirit, the simplest of a long series of organic compounds called alcohols, consisting of a methyl group (CH3) linked with a hydroxy group (OH). Methanol was formerly produced by the destructive distillation of wood.
How will you prepare 2 Phenylpropane 2 OL from acetone?
Acetone react with Phenylmagnesium bromide to form 2-phenyl propan-2-ol.
How do you use resorcinol?
Apply enough resorcinol to cover the affected areas, and rub in gently. Immediately after using this medicine, wash your hands to remove any medicine that may be on them. Keep this medicine away from the eyes. If you should accidentally get some in your eyes, flush them thoroughly with water.