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137995

1,2,3-Trimethoxybenzene

Name: 1,2,3-Trimethoxybenzene
Brand: ALDRICH

98%

Synonym(s):

Pyrogallol trimethyl ether

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About This Item

Linear Formula:

C₆H₃(OCH₃)₃

CAS Number:

634-36-6

Molecular Weight:

168.19

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24848225

EC Number:

211-207-2

Beilstein/REAXYS Number:

1910422

MDL number:

MFCD00008358

Assay:

98%

Form:

chunks

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Properties

Quality Level

100

assay

98%

form

chunks

bp

241 °C (lit.)

mp

43-47 °C (lit.)

density

1.112 g/mL at 25 °C (lit.)

SMILES string

COc1cccc(OC)c1OC

InChI

1S/C9H12O3/c1-10-7-5-4-6-8(11-2)9(7)12-3/h4-6H,1-3H3

InChI key

CRUILBNAQILVHZ-UHFFFAOYSA-N

Description

General description

1,2,3-Trimethoxybenzene on condensation with 2,4-diamino-5-(hydroxymethyl)pyrimidine yields 2,4-diamino-5-(2,3,4-trimethoxybenzyl)pyrimidine.

Application

1,2,3-Trimethoxybenzene was used to study the effect of solvent on photoinduced electron-transfer reactions.

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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Mono, bis, and tris(phosphoramidate) titanium complexes: synthesis, structure, and reactivity investigations.

Mitchell R Perry et al.

Dalton transactions (Cambridge, England : 2003), 48(26), 9782-9790 (2019-05-10)

A series of variously substituted phosphoramidate titanium complexes bearing dimethylamido ligands are reported. Aryl-substituted ligands impart crystallinity to the systems and allow for the elucidation of the molecular structures via X-ray crystallography. Higher-substituted complexes, including a tris(phosphoramidate)mono(dimethylamido) complex, were isolated

A high-resolution (13)C 3D CSA-CSA-CSA correlation experiment by means of magic angle turning.

J Z Hu et al.

Journal of magnetic resonance (San Diego, Calif. : 1997), 145(2), 230-236 (2000-07-27)

It is shown in this paper that a previously reported 90 degrees sample flipping (13)C 2D CSA-CSA correlation experiment may be carried out alternatively by employing constant slow sample rotation about the magic angle axis and by synchronizing the read

2,4-diamino-5-benzylpyrimidines and analogues as antibacterial agents. 6. A one-step synthesis of new trimethoprim derivatives and activity analysis by molecular modeling.

A Stuart et al.

Journal of medicinal chemistry, 26(5), 667-673 (1983-05-01)

A new route to 2,4-diamino-5-(4-hydroxybenzyl)pyrimidines has been developed that involves the condensation of 2,4-diamino-5-(hydroxymethyl)pyrimidine with phenols in acidic medium. The use of phenol and its 2,6-dialkyl derivatives produces 5-(4-hydroxybenzyl)pyrimidines exclusively. However, 2,6-dimethoxyphenol produces a mixture of 5-(3-hydroxy-2,4-dimethoxybenzyl)- and 5-(4-hydroxy-3,5-dimethoxybenzyl)pyrimidines. The

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Global Trade Item Number

SKU	GTIN
137995-100G	04061838345943
137995-25G	04061838732163