Skip to Content
Merck
CN

Key Documents

View All Documentation

138711

2,4,6-Trimethoxybenzaldehyde

98%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(CH3O)3C6H2CHO
CAS Number:
830-79-5
Molecular Weight:
196.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848365
EC Number:
212-598-2
Beilstein/REAXYS Number:
1956051
MDL number:
MFCD00003313
Assay:
98%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

100

assay

98%

form

solid

mp

115-120 °C (lit.)

functional group

aldehyde

SMILES string

[H]C(=O)c1c(OC)cc(OC)cc1OC

InChI

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

InChI key

CRBZVDLXAIFERF-UHFFFAOYSA-N

General description

2,4,6-Trimethoxybenzaldehyde exhibits significant anti-candida activity.

Application

2,4,6-Trimethoxybenzaldehyde was used in the preparation and characterization of three RNA-specifc fluorescent probes (E36, E144 and F22) and their use in live cell imaging. It was used as starting reagent for the regioselective synthesis of new (+/-)-8-alkyl-5,7-dihydroxy-4-(4-hydroxyphenyl)-3,4-dihydrocoumarins.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000244701
MKCS5041
0000244701
MKBZ3019V
MKBT8374V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Sandeep B Rajput et al.
Chinese medicine, 8(1), 18-18 (2013-09-10)
Asaronaldehyde (2, 4, 5-trimethoxybeznaldehyde) is an active component of Acorus gramineus rhizome. This study aims to evaluate the anti-Candida efficacy of asaronaldehyde and its three structural isomers, namely, 2, 3, 4-trimethoxybenzaldehyde, 3, 4, 5-trimethoxybenzaldehyde, and 2, 4, 6- trimethoxybenzaldehyde. Susceptibility
Asma Alshamari et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-24)
A series of derivatives of trans-3-(2,4,6-trimethoxyphenyl)4,5-dihydroisoxazolo-4,5-bis[carbonyl-(4'phenyl)thiosemicarbazide (9) and of trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro isoxazolo-4,5-bis(aroylcarbohydrazide) (10a-c) were synthesized from trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro-4,5-bis(hydrazenocarbonyl)isoxazole (8). The structures of the compounds were elucidated by both elemental and spectral (IR, NMR, and MS) analysis. Compound 9 shows activity against some
Fatemeh Oroojalian et al.
Journal of controlled release : official journal of the Controlled Release Society, 288, 45-61 (2018-09-02)
In the current study, thermoresponsive poly(N-isopropylacrylamide)-doxorubicin (PNIPAM-DOX) hydrogel was synthesized and loaded into pH-responsive poly ethylene glycol)-2,4,6- trimethoxy benzylidene pentaerythritol carbonate (PEG-PTMBPEC) polymersomes in order to fabricate a smart thermo-pH stimuli responsive drug delivery system. Thermo-pH responsive polymersomal formulation of
View All Related Papers

Global Trade Item Number

SKUGTIN
138711-50G04061838732446
138711-10G04061838732439