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91-52-1

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91-52-1 Usage

Chemical Properties

white to off-white powder

Uses

Yttrium and heavy lanthanide complexes is synthesised with 2, 4-dimethoxybenzoic acid and thermal and spectral features is studied. In the case of the electron-rich aromatic system 2,4-dimethoxybenzoic acid reduction of the intermediate HOBt ester is slow, and good.

Purification Methods

Crystallise the acid from water and dry it in a vacuum desiccator over H2SO4.. The S-benzylisothiuronium salt has m 158-159o (from CHCl3). [Beilstein 10 H 379, 10 I 177, 10 II 252, 10 III 1371, 10 IV 1422.] Aromatic acid impurities (to <0.05%) can be removed via the (±)--methylbenzylamine salt as described for 2,4-dichlorobenzoic acid [Ley & Yates Organic Process Research & Development 12 120 2008.]

Check Digit Verification of cas no

The CAS Registry Mumber 91-52-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91-52:
(4*9)+(3*1)+(2*5)+(1*2)=51
51 % 10 = 1
So 91-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O4/c1-12-6-3-4-7(9(10)11)8(5-6)13-2/h3-5H,1-2H3,(H,10,11)/p-1

91-52-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A16252)  2,4-Dimethoxybenzoic acid, 98%   

  • 91-52-1

  • 25g

  • 292.0CNY

  • Detail
  • Alfa Aesar

  • (A16252)  2,4-Dimethoxybenzoic acid, 98%   

  • 91-52-1

  • 100g

  • 995.0CNY

  • Detail

91-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dimethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names O,O-dimethylresorcilic 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:91-52-1 SDS

91-52-1Relevant articles and documents

Continuous production method of benzoic acid derivative

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Paragraph 0032-0034, (2021/11/14)

The invention relates to the technical field of preparation of benzoic acid derivatives. The invention particularly relates to a continuous production method of a benzoic acid derivative. The continuous reaction device is characterized by comprising a small-diameter sleeve, wherein the small-diameter sleeve is sleeved with a large-diameter sleeve, and a small pipeline is arranged between the small-diameter sleeve and the large-diameter sleeve, and a plurality of small holes are arranged on the small pipeline. The small-diameter casing is rotated, the large-diameter casing is fixed, and the reaction liquid composed of the nitric acid and the toluene derivative is between a small-diameter casing pipe and a large-diameter casing pipe.

Silver-catalyzed decarboxylative homocoupling reaction for the construction of tetrafluoroethylene-bridging aromatic compounds

Wang, Yong,Zhao, Huaxin,Xie, Xiaojuan,Jiang, Haizhen,Deng, Hongmei,Hao, Jian,Wan, Wen

supporting information, p. 2961 - 2970 (2019/08/22)

The Ag(I)-catalyzed decarboxylative homocoupling from the difluoroacetate has been developed to the synthesis of symmetric CF2–CF2 containing dimers. This radical dimerization overpasses the prefunctionalization of the substrate and provides a direct and efficient method for construction of tetrafluoroethylene bridge-linked homodimers.

A mild method for synthesizing carboxylic acids by oxidation of aldoximes using hypervalent iodine reagents

Nakamura, Akira,Kanou, Hodaka,Tanaka, Junki,Imamiya, Akira,Maegawa, Tomohiro,Miki, Yasuyoshi

supporting information, p. 541 - 544 (2018/02/07)

A mild oxidation method for the conversion of aldoximes to carboxylic acids was developed mediated by hypervalent iodine reagents. This method covers a wide range of functionalized aldoximes and proceeds under mild conditions, utilizing PhI(OH)OTs as an oxidant.

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