| Identification | More | [Name]
2,3-Dimethoxybenzaldehyde | [CAS]
86-51-1 | [Synonyms]
2,3-DIMETHOXYBENZALDEHYDE
2-VERATRALDEHYDE
AKOS BBS-00003161
BENZALDEHYDE, 2,3-DIMETHOXY-
LABOTEST-BB LT00932325
O-VERATRALDEHYDE
O-VERATRIC ALDEHYDE
3,5-Dihydroxypropiophenone
3,5-Dimethylsalicylic acid
4-Diethoxybenzene
2,3-Dimethoxybenzenecarbonal
2,3-Dimethoxybenzaldehyde 97%
2,3-DIMETHOXYBENZALDEHYDE(3,5-DIMETHYLSALICYLICACID)
2,3-dlmethoxybenzaldehyde
Orthoveratraldehyde
2,3-Dimethoxybenzaldehyde, 98+% | [EINECS(EC#)]
201-677-7 | [Molecular Formula]
C9H10O3 | [MDL Number]
MFCD00003309 | [Molecular Weight]
166.17 | [MOL File]
86-51-1.mol |
| Chemical Properties | Back Directory | [Appearance]
white to brown crystalline powder | [Melting point ]
48-52 °C (lit.) | [Boiling point ]
137 °C/12 mmHg (lit.) | [density ]
1.1708 (rough estimate) | [refractive index ]
1.5500 (estimate) | [Fp ]
>230 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
Solubility in methanol with almost transparency. | [form ]
Crystalline Powder, Crystals, and/or Chunks | [color ]
Off-white to beige | [Sensitive ]
Air Sensitive | [BRN ]
908264 | [InChIKey]
JIVGSHFYXPRRSZ-UHFFFAOYSA-N | [LogP]
1.630 (est) | [CAS DataBase Reference]
86-51-1(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzaldehyde, 2,3-dimethoxy-(86-51-1) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
CU5732000 | [Hazard Note ]
Irritant | [HS Code ]
29124900 | [Safety Profile]
A poison by ingestion.
When heated to decomposition it emits
acrid smoke and irritating vapors |
| Hazard Information | Back Directory | [Chemical Properties]
white to brown crystalline powder | [Uses]
A benzaldehyde derivative that may possess antifungal activity of redox-active benzaldehydes that target cellular antioxidation. It could function as chemosensitizing agents in concert with convention
al drugs or fungicides to improve antifungal efficacy. |
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