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161713

Sigma-Aldrich

3,5-Dimethoxybenzoyl chloride

97%

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About This Item

Linear Formula:
(CH3O)2C6H3COCl
CAS Number:
17213-57-9
Molecular Weight:
200.62
Beilstein:
511839
EC Number:
241-256-5
MDL number:
MFCD00000676
UNSPSC Code:
12352100
PubChem Substance ID:
24849950
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

bp

157-158 °C/16 mmHg (lit.)

mp

43-46 °C (lit.)

functional group

acyl chloride

SMILES string

COc1cc(OC)cc(c1)C(Cl)=O

InChI

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

InChI key

FTHPLWDYWAKYCY-UHFFFAOYSA-N

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General description

3,5-Dimethoxybenzoyl chloride undergoes addition reaction with 4,4-dimethyl-2-pentyne in presence of AlCl3 via 1,2- methyl shift.

Application

3,5-Dimethoxybenzoyl chloride was used to study the mechanism and kinetics of solvolysis of 3,4- and 3,5-dimethoxybenzoyl chlorides in various binary solvents.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

161713-BULK:
161713-1KG:
161713-VAR:
161713-50G:
161713-10G:

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Certificates of Analysis (COA)

Lot/Batch Number
STBD3016V
STBB0830
S41086
17126BH
06313BH

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Kinetic and Theoretical Consideration of 3, 4-and 3, 5-Dimethoxybenzoyl Chlorides Solvolyses.
Park K-H and Kevill DN.
Bull. Korean Chem. Soc., 34(10), 2989-2989 (2013)
Stereochemistry and mechanism of acylation of acetylenes.
Martens H, et al.
Tetrahedron, 31(2), 177-183 (1975)
Dongsheng Xu et al.
Journal of chromatography. A, 1593, 63-72 (2019-02-05)
An O-[2-(methacryloyloxy)-ethylcarbamoyl]-10,11-dihydroquinidine (MQD)-silica hybrid monolithic column was prepared by a facile "one-step" strategy within a 100 μm I.D. capillary. The influence of the methanol, ethylene glycol and water volume ratio, reaction temperature and time, cetyltrimethylammonium bromide and MQD monomers content

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