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17213-57-9

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17213-57-9 Usage

Chemical Properties

off-white to light brown crystalline powder

Uses

Different sources of media describe the Uses of 17213-57-9 differently. You can refer to the following data:
1. 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. 3,5-Dimethoxybenzoyl chloride undergoes addition reaction with 4,4-dimethyl-2-pentyne in presence of AlCl3 via 1,2- methyl shift. It is used as a chemical and organic intermediate.
2. 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.

General Description

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

Check Digit Verification of cas no

The CAS Registry Mumber 17213-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,1 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17213-57:
(7*1)+(6*7)+(5*2)+(4*1)+(3*3)+(2*5)+(1*7)=89
89 % 10 = 9
So 17213-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO3/c1-12-7-3-6(9(10)11)4-8(5-7)13-2/h3-5H,1-2H3

17213-57-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (D2609)  3,5-Dimethoxybenzoyl Chloride  >98.0%(GC)(T)

  • 17213-57-9

  • 5g

  • 455.00CNY

  • Detail
  • TCI America

  • (D2609)  3,5-Dimethoxybenzoyl Chloride  >98.0%(GC)(T)

  • 17213-57-9

  • 25g

  • 1,320.00CNY

  • Detail
  • Alfa Aesar

  • (A14744)  3,5-Dimethoxybenzoyl chloride, 98%   

  • 17213-57-9

  • 5g

  • 669.0CNY

  • Detail
  • Alfa Aesar

  • (A14744)  3,5-Dimethoxybenzoyl chloride, 98%   

  • 17213-57-9

  • 25g

  • 2166.0CNY

  • Detail
  • Alfa Aesar

  • (A14744)  3,5-Dimethoxybenzoyl chloride, 98%   

  • 17213-57-9

  • 100g

  • 7354.0CNY

  • Detail
  • Aldrich

  • (161713)  3,5-Dimethoxybenzoylchloride  97%

  • 17213-57-9

  • 161713-10G

  • 964.08CNY

  • Detail
  • Aldrich

  • (161713)  3,5-Dimethoxybenzoylchloride  97%

  • 17213-57-9

  • 161713-50G

  • 2,975.31CNY

  • Detail

17213-57-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-DIMETHOXYBENZOYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 3,5-dimethoxybenzoic acid chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17213-57-9 SDS

17213-57-9Relevant articles and documents

-

Bycroft,Roberts

, p. 2063,2064 (1962)

-

Palladium-Catalyzed Chlorocarbonylation of Aryl (Pseudo)Halides Through In Situ Generation of Carbon Monoxide

Bismuto, Alessandro,Boehm, Philip,Morandi, Bill,Roediger, Sven

supporting information, p. 17887 - 17896 (2020/08/19)

An efficient palladium-catalyzed chlorocarbonylation of aryl (pseudo)halides that gives access to a wide range of carboxylic acid derivatives has been developed. The use of butyryl chloride as a combined CO and Cl source eludes the need for toxic, gaseous carbon monoxide, thus facilitating the synthesis of high-value products from readily available aryl (pseudo)halides. The combination of palladium(0), Xantphos, and an amine base is essential to promote this broadly applicable catalytic reaction. Overall, this reaction provides access to a great variety of carbonyl-containing products through in situ transformation of the generated aroyl chloride. Combined experimental and computational studies support a reaction mechanism involving in situ generation of CO.

Wavelength-Orthogonal Photocleavable Monochromophoric Linker for Sequential Release of Two Different Substrates

Venkatesh, Yarra,Chaudhuri, Amrita,Mondal, Saugat,Shah, Sk. Sheriff,Singh, N. D. Pradeep

, p. 295 - 299 (2020/01/02)

A wavelength-orthogonal photocleavable monochromophoric linker was developed that is based on a 3-acetyl-9-ethyl-6-methylcarbazole (AEMC) moiety substituted at both the phenacyl and benzylic positions with different carboxylic acids. The different carboxylic acids were released sequentially upon irradiation with light of λ ≥ 365 nm and λ ≥ 290 nm, respectively.

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