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Names | |
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Preferred IUPAC name
Phenylmethanediol | |
Other names
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Identifiers | |
3D model (
JSmol)
|
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ChemSpider | |
PubChem
CID
|
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CompTox Dashboard (
EPA)
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Properties | |
C7H8O2 | |
Molar mass | 124.139 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Phenylmethanediol is an organic compound that is a geminal diol, the hydrate of benzaldehyde. It is a short-lived intermediate in some chemical reactions, such as oxidations of toluene [2] and benzaldehyde [3] and the reduction of benzoic acid. [4]
{{
cite journal}}
: CS1 maint: multiple names: authors list (
link)
{{
cite journal}}
: CS1 maint: multiple names: authors list (
link)
![]() | |
Names | |
---|---|
Preferred IUPAC name
Phenylmethanediol | |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C7H8O2 | |
Molar mass | 124.139 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Phenylmethanediol is an organic compound that is a geminal diol, the hydrate of benzaldehyde. It is a short-lived intermediate in some chemical reactions, such as oxidations of toluene [2] and benzaldehyde [3] and the reduction of benzoic acid. [4]
{{
cite journal}}
: CS1 maint: multiple names: authors list (
link)
{{
cite journal}}
: CS1 maint: multiple names: authors list (
link)