Key Documents

View All Documentation

258040

3,4-Dimethoxybenzoyl chloride

Name: 3,4-Dimethoxybenzoyl chloride
Brand: ALDRICH

98%

Synonym(s):

Veratroyl chloride

Select a Size

Change View

About This Item

Linear Formula:

(CH₃O)₂C₆H₃COCl

CAS Number:

3535-37-3

Molecular Weight:

200.62

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24855625

EC Number:

222-568-0

Beilstein/REAXYS Number:

783596

MDL number:

MFCD00000674

Assay:

98%

Form:

solid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

98%

form

solid

mp

70-73 °C (lit.)

functional group

acyl chloride

SMILES string

COc1ccc(cc1OC)C(Cl)=O

InChI

1S/C9H9ClO3/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3

InChI key

VIOBGCWEHLRBEP-UHFFFAOYSA-N

Description

Application

3,4-Dimethoxybenzoyl chloride has been used in synthesis of:

(+)-5-(3,4-dimethoxyphenyl)-4-[[N-[(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]]carbonyl] oxazole and its enantiomer
N-(2,5-dibromophenyl)-3,4-dimethoxybenzamide

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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

Chiral Auxiliary-Bearing Isocyanides as Synthons: Synthesis of Strongly Fluorescent (+)-5-(3,4-Dimethoxyphenyl)-4-[[N- [(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]]carbonyl]oxazole and Its Enantiomer.

Jian S. Tang et al.

The Journal of organic chemistry, 61(25), 8750-8754 (1996-12-13)

Both (4S-(+)-3-(isocyanoacetyl)-4-(phenylmethyl)-2-oxazolidinone (R)-1 and its enantiomer (S)-1 have been synthesized as potentially useful synthons in asymmetric synthesis. Optically active (+)-5-(3,4-dimethoxyphenyl)-4-[[N-[(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]]carbonyl] oxazole (S)-2 and its enantiomer (R)-2 obtained by treating 3,4-dimethoxybenzoyl chloride with (S)-1 and (R)-1, respectively, in the presence of

Antitumor benzothiazoles. 26.(1) 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (GW 610, NSC 721648), a simple fluorinated 2-arylbenzothiazole, shows potent and selective inhibitory activity against lung, colon, and breast cancer cell lines.

Catriona G Mortimer et al.

Journal of medicinal chemistry, 49(1), 179-185 (2006-01-06)

A series of new 2-phenylbenzothiazoles has been synthesized on the basis of the discovery of the potent and selective in vitro antitumor properties of 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (8n; GW 610, NSC 721648). Synthesis of analogues substituted in the benzothiazole ring was achieved