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603-79-2

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603-79-2 Usage

Chemical Properties

white to light yellow crystal powder

Uses

2,3-Dimethylbenzoic Acid is used as a reagent in the synthesis of pyridyl benzamides as inhibitors for the kinetoplastid Trypanosoma brucei. 2,3-Dimethylbenzoic Acid is also used as a reagent in the synthesis of 2,3-Dihydro-1H-isoindole-4-carboxylic Acid (D450070) which is a reagent used in the synthesis of aminoalkylbenzoic acid derivatives for the treatment of faintness attacks, hypokinesia, cranial disorders, neurodegenerative disorders, depression, anxiety, neuropathic pain, neuropathological disorders and sleep disorders.

Definition

ChEBI: A dimethylbenzoic acid in which the two methyl groups are located at positions 2 and 3.

General Description

2,3-Dimethylbenzoic acid shows high binding affinity with antenna-specific odorant-binding protein of the alfalfa plant bug, Adelphocoris lineolatus.

Purification Methods

Crystallise the acid from EtOH. It is volatile in steam. The amide has m 156o (from H2O). [Beilstein 9 H 531, 9 III 2434, 9 IV 1797.]

Check Digit Verification of cas no

The CAS Registry Mumber 603-79-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 603-79:
(5*6)+(4*0)+(3*3)+(2*7)+(1*9)=62
62 % 10 = 2
So 603-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O2/c1-6-4-3-5-8(7(6)2)9(10)11/h3-5H,1-2H3,(H,10,11)/p-1

603-79-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A10383)  2,3-Dimethylbenzoic acid, 98%   

  • 603-79-2

  • 5g

  • 526.0CNY

  • Detail
  • Alfa Aesar

  • (A10383)  2,3-Dimethylbenzoic acid, 98%   

  • 603-79-2

  • 25g

  • 2200.0CNY

  • Detail
  • Alfa Aesar

  • (A10383)  2,3-Dimethylbenzoic acid, 98%   

  • 603-79-2

  • 100g

  • 7387.0CNY

  • Detail

603-79-2SDS

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 2,3-dimethylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2,3-Dimethylbenzoic 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:603-79-2 SDS

603-79-2Relevant articles and documents

ISOINDOLINONE COMPOUNDS

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Page/Page column 206, (2021/04/17)

Disclosed herein is a compound or pharmaceutically acceptable salts or stereoisomers thereof of of formula I wherein X1 is linear or branched C1-6 alkyl, C3-6 cycloalkyl, -C1-6 alkyl C3-6 cycloalkyl, C6-10 aryl, 5-10 membered heteroaryl, C1-6 alkyl C6-10 aryl, C1-6 alkyl 5-10 membered heteroaryl, wherein X1 is unsubstituted or substituted with one or more of halogen, linear or branched C1-6 alkyl, linear or branched C1-6 heteroalkyl, CF3, CHF2, -O-CHF2, -O-(CH2)2-OMe, OCF3, C1-6 alkylamino, -CN, -N(H)C(O)-C1- 6alkyl, -OC(O)-C1-6alkyl, -OC(O)-C1-4alkylamino, -C(O)O-C1-6alkyl, -COOH, - CHO, -C1-6alkylC(O)OH, -C1-6alkylC(O)O-C1-6alkyl, NH2, C1-6 alkoxy or C1-6 alkylhydroxy; X2 is hydrogen, C6-10 aryl, 5-10 membered heteroaryl, -O-(5-10 membered heteroaryl), 4-8 membered heterocycloalkyl, C1-4 alkyl 4-8 membered heterocycloalkyl, -O-(4-8 membered heterocycloalkyl), -O-C1-4 alkyl-(4-8 membered heterocycloalkyl), -OC(O)-C1-4alkyl-4-8 membered heterocycloalkyl or C6 aryloxy, wherein X2 is unsubstituted or substituted with one or more of linear or branched C1-6 alkyl, NH2, NMe2 or 5-6 membered heterocycloalkyl; n is 0, 1 or 2.

Method for preparing aromatic acid by direct carboxylation of CO2

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Paragraph 0059; 0060, (2018/05/16)

The invention discloses a method for preparing aromatic acid by direct carboxylation of CO2. The method comprises the following steps: (1) adding aromatic hydrocarbon, organic alkali and lewis acid into a high pressure reaction kettle under an inert gas atmosphere, then feeding CO2 gas into the high pressure reaction kettle for reaction, and obtaining reaction liquid with aromatic acid at the endof the reaction; (2) adding water into the reaction liquid obtained in the step (1), then extracting the aromatic acid in the reaction liquid with an extracting agent to enable the aromatic acid in the reaction liquid to enter an extracting phase, separating the extracting phase from raffinate, and concentrating the extracting phase to obtain the aromatic acid. According to the method, complicatedpreparation of ionic liquid is avoided, and organic alkali is timely neutralized with halogen hydride produced by the reaction, so that the balance moves rightwards; at the end of the reaction, the organic alkali also can be recycled through alkali treatment. The method has the advantages of simple operation, mild conditions, green process, low cost and the like, and is expected to be applied toindustrial production.

Inclusion complex containing epoxy resin composition for semiconductor encapsulation

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, (2014/03/21)

The invention is an epoxy resin composition for sealing a semiconductor, including (A) an epoxy resin and (B) a clathrate complex. The clathrate complex is one of (b1) an aromatic carboxylic acid compound, and (b2) at least one imidazole compound represented by formula (II): wherein R2 represents a hydrogen atom, C1-C10 alkyl group, phenyl group, benzyl group or cyanoethyl group, and R3 to R5 represent a hydrogen atom, nitro group, halogen atom, C1-C20 alkyl group, phenyl group, benzyl group, hydroxymethyl group or C1-C20 acyl group. The composition has improved storage stability, retains flowability when sealing, and achieves an effective curing rate applicable for sealing delicate semiconductors.

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