126292
3,5-Dimethoxybenzaldehyde
98%
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About This Item
Linear Formula:
(CH3O)2C6H3CHO
CAS Number:
Molecular Weight:
166.17
MDL number:
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-772-6
Beilstein/REAXYS Number:
2042374
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
bp
151 °C/16 mmHg (lit.)
mp
45-48 °C (lit.)
functional group
aldehyde
SMILES string
[H]C(=O)c1cc(OC)cc(OC)c1
InChI
1S/C9H10O3/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-6H,1-2H3
InChI key
VFZRZRDOXPRTSC-UHFFFAOYSA-N
Application
Used frequently as synthetic building block.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>233.6 °F
flash_point_c
> 112 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Marco Bandini et al.
Organic letters, 9(11), 2151-2153 (2007-05-08)
A new poly(ethylene glycol)-modified DAT2-Cu(OAc)2 complex smoothly catalyzes a base-free nitroaldol condensation in a highly enantioselective manner (ee up to 93%) also in reagent-grade solvent and in the presence of air. Effective recovery and recycling (up to five runs) of
Johannes Taeger et al.
Oncology letters, 16(1), 654-659 (2018-06-22)
Despite partial advances in therapy for patients suffering from head and neck squamous cell carcinomas (HNSCC), prognosis still remains poor with minimal improvement in survival for over the last several decades. Some agents found are known to cause cancer cell
Katie A Keaton et al.
Organic letters, 9(14), 2717-2719 (2007-06-15)
A strategy for ketone synthesis with cyclopropanols as intermediates and its application to (+)-spirolaxine methyl ether is described. The synthesis also features an application of Fu's alkyl-alkyl Suzuki coupling.