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Merck
CN

152099

2,3,4-Trimethoxybenzaldehyde

99%

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About This Item

Linear Formula:
(CH3O)3C6H2CHO
CAS Number:
Molecular Weight:
196.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-271-0
Beilstein/REAXYS Number:
981091
MDL number:
Assay:
99%
Form:
solid
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InChI key

UCTUXUGXIFRVGX-UHFFFAOYSA-N

InChI

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

SMILES string

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

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

Quality Level

Application

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


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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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