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126292

3,5-Dimethoxybenzaldehyde

98%

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About This Item

Linear Formula:
(CH3O)2C6H3CHO
CAS Number:
7311-34-4
Molecular Weight:
166.17
MDL number:
MFCD00003366
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847713
EC Number:
230-772-6
Beilstein/REAXYS Number:
2042374
Assay:
98%
Form:
solid

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InChI key

VFZRZRDOXPRTSC-UHFFFAOYSA-N

InChI

1S/C9H10O3/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-6H,1-2H3

SMILES string

[H]C(=O)c1cc(OC)cc(OC)c1

assay

98%

form

solid

bp

151 °C/16 mmHg (lit.)

mp

45-48 °C (lit.)

functional group

aldehyde

Quality Level

100

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This Item
D130206D130400T68403
3,5-Dimethoxybenzaldehyde 98%

Sigma-Aldrich

126292

3,5-Dimethoxybenzaldehyde

2,3-Dimethoxybenzaldehyde 98%

Sigma-Aldrich

D130206

2,3-Dimethoxybenzaldehyde

2,4-Dimethoxybenzaldehyde 98%

Sigma-Aldrich

D130400

2,4-Dimethoxybenzaldehyde

3,4,5-Trimethoxybenzaldehyde 98%

Sigma-Aldrich

T68403

3,4,5-Trimethoxybenzaldehyde

assay

98%

assay

98%

assay

98%

assay

98%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

200

form

solid

form

crystals

form

crystals

form

-

bp

151 °C/16 mmHg (lit.)

bp

137 °C/12 mmHg (lit.)

bp

165 °C/10 mmHg (lit.)

bp

163-165 °C/10 mmHg (lit.)

mp

45-48 °C (lit.)

mp

48-52 °C (lit.)

mp

67-69 °C (lit.)

mp

72-74 °C (lit.)

functional group

aldehyde

functional group

-

functional group

-

functional group

-

Application

Used frequently as synthetic building block.[1][2]

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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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6665
STBD1234V
STBC8619V
STBC7941V
STBC7337V

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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
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.
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
Kirsti Parikka et al.
Beilstein journal of organic chemistry, 5, 22-22 (2009-07-11)
The first synthesis of bioactive long alkyl chain 5-n-alkylresorcinols, present in whole grain products, by a novel modification of the Wittig reaction is described. All the main long chain 5-n-alkylresorcinols present in rye and wheat, including C(23) and C(25) analogues
Monika Osińska-Jaroszuk et al.
Bioprocess and biosystems engineering, 41(7), 973-989 (2018-03-28)
Four bacterial EPSs extracted from Rhizobium leguminosarum bv. trifolii Rt24.2, Sinorhizobium meliloti Rm1021, Bradyrhizobium japonicum USDA110, and Bradyrhizobium elkanii USDA76 were determined towards their metal ion adsorption properties and possible modification of Cerrena unicolor laccase properties. The highest magnesium and
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