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152099

Sigma-Aldrich

2,3,4-Trimethoxybenzaldehyde

99%

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About This Item

Linear Formula:
(CH3O)3C6H2CHO
CAS Number:
2103-57-3
Molecular Weight:
196.20
Beilstein:
981091
EC Number:
218-271-0
MDL number:
MFCD00003310
UNSPSC Code:
12352100
PubChem Substance ID:
24849197
NACRES:
NA.22

Quality Level

100

Assay

99%

form

solid

refractive index

n20/D 1.5547 (lit.)

bp

168-170 °C/12 mmHg (lit.)

mp

38-40 °C (lit.)

functional group

aldehyde

SMILES string

[H]C(=O)c1ccc(OC)c(OC)c1OC

InChI

1S/C10H12O4/c1-12-8-5-4-7(6-11)9(13-2)10(8)14-3/h4-6H,1-3H3

InChI key

UCTUXUGXIFRVGX-UHFFFAOYSA-N

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Application

2,3,4-Trimethoxybenzaldehyde was used to study the effects of 2,3,4-trimethoxybenzaldehyde on tubulin-dependent GTP hydrolysis.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6351
STBH8754
STBH0736
STBF5274V
STBD8973V

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C M Lin et al.
The Journal of biological chemistry, 256(17), 9242-9245 (1981-09-10)
The effects of a number of antimitotic drugs on the GTPase activity of tubulin were examined. The previously reported stimulation with colchicine and inhibition with podophyllotoxin and vinblastine wee confirmed. Maytansine, which competes with vinblastine in binding to tubulin, was

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