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1132-21-4

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1132-21-4 Usage

Chemical Properties

almost white to light beige-pink cryst. powder

Uses

3,5-Dimethoxybenzoic acid (3,5-DmeoxBA) can be used as a reactant for the synthesis of:5,7-Dimethoxy-3,4-diphenylisocoumarin by coupling with diphenylacetylene.Biotin dimedone, a reagent used in the study of protein sulfenation.It can also be used as a ligand to synthesize lanthanide complexes [Ln(3,5-DmeoxBA)3(phen)]2; where phen is 1,10-phenanthroline.

Purification Methods

Crystallise the acid from water, EtOH or aqueous acetic acid and dry it in a vacuum. [Beilstein 10 H 405, 10 I 195, 10 III 1446, 10 IV 1501.]

Check Digit Verification of cas no

The CAS Registry Mumber 1132-21-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1132-21:
(6*1)+(5*1)+(4*3)+(3*2)+(2*2)+(1*1)=34
34 % 10 = 4
So 1132-21-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O4/c1-12-7-3-6(9(10)11)4-8(5-7)13-2/h3-5H,1-2H3,(H,10,11)/p-1

1132-21-4 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (D1534)  3,5-Dimethoxybenzoic Acid  >98.0%(GC)(T)

  • 1132-21-4

  • 25g

  • 350.00CNY

  • Detail
  • TCI America

  • (D1534)  3,5-Dimethoxybenzoic Acid  >98.0%(GC)(T)

  • 1132-21-4

  • 500g

  • 2,990.00CNY

  • Detail
  • Alfa Aesar

  • (A14374)  3,5-Dimethoxybenzoic acid, 99%   

  • 1132-21-4

  • 25g

  • 372.0CNY

  • Detail
  • Alfa Aesar

  • (A14374)  3,5-Dimethoxybenzoic acid, 99%   

  • 1132-21-4

  • 100g

  • 915.0CNY

  • Detail
  • Alfa Aesar

  • (A14374)  3,5-Dimethoxybenzoic acid, 99%   

  • 1132-21-4

  • 500g

  • 4154.0CNY

  • Detail

1132-21-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Dimethoxybenzoic Acid

1.2 Other means of identification

Product number -
Other names 3,5-Dimethoxybenzoic acid

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:1132-21-4 SDS

1132-21-4Relevant articles and documents

-

Meyer,H.

, p. 429 (1887)

-

Dicarbonyl chelates from 1-cymantrenylalkylamides with the dendrite structure: formation, photochromism, and kinetics of dark reaction with carbon monoxide

Kelbysheva,Telegina,Abramova,Strelkova,Ikonnikov,Rodionov,Ezernitskaya,Lokshin,Loim

, p. 2646 - 2654 (2015)

Photolysis of carboxamides of the dendrite structure with aminomethyland 1-aminoethylcymantrenes leads to the formation of six-membered dicarbonyl chelates with the Mn—O bond which are stable in solutions. The chelates in the reversed dark reaction with carbon monoxide give the starting tricarbonyl complexes. The formation of the chelates and their dark reaction are accompanied by the reversible change of color by the compounds. The rate determining step of the thermal reaction of chelates with CO is a chelate ring opening with the ligand substitution by the SN1 mechanism. A possibility of solvent-free photoinduced ligand-exchange reaction in a number of cymantrene derivatives was demonstrated.

The Continuous-Flow Synthesis of Carboxylic Acids using CO2 in a Tube-In-Tube Gas Permeable Membrane Reactor

Polyzos, Anastasios,O'Brien, Matthew,Petersen, Trine P.,Baxendale, Ian R.,Ley, Steven V.

, p. 1190 - 1193 (2011)

Keep it simple: A gas-liquid flow reactor has been developed based on a gas permeable tube-in-tube configuration which effectively delivers gas to a liquid substrate stream in a safe, continuous fashion. A series of carboxylic acids were prepared from the reaction of CO2 with a range of Grignard reagents (see picture).

One-Pot Direct Oxidation of Primary Amines to Carboxylic Acids through Tandem ortho-Naphthoquinone-Catalyzed and TBHP-Promoted Oxidation Sequence

Kim, Hun Young,Oh, Kyungsoo,Si, Tengda

supporting information, p. 18150 - 18155 (2021/12/09)

Biomimetic oxidation of primary amines to carboxylic acids has been developed where the copper-containing amine oxidase (CuAO)-like o-NQ-catalyzed aerobic oxidation was combined with the aldehyde dehydrogenase (ALDH)-like TBHP-mediated imine oxidation protocol. Notably, the current tandem oxidation strategy provides a new mechanistic insight into the imine intermediate and the seemingly simple TBHP-mediated oxidation pathways of imines. The developed metal-free amine oxidation protocol allows the use of molecular oxygen and TBHP, safe forms of oxidant that may appeal to the industrial application.

Cobalt-catalyzed carboxylation of aryl and vinyl chlorides with CO2

Wang, Yanwei,Jiang, Xiaomei,Wang, Baiquan

supporting information, p. 14416 - 14419 (2020/12/01)

The transition-metal-catalyzed carboxylation of aryl and vinyl chlorides with CO2 is rarely studied, and has been achieved only with a Ni catalyst or combination of palladium and photoredox. In this work, the cobalt-catalyzed carboxylation of aryl and vinyl chlorides and bromides with CO2 has been developed. These transformations proceed under mild conditions and exhibit a broad substrate scope, affording the corresponding carboxylic acids in good to high yields.

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