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4919-37-3

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4919-37-3 Usage

Description

4-Hydroxy-3,5-dimethylbenzoic acid is an organic compound characterized by its off-white to light pink or light beige crystalline appearance. It is a derivative of benzoic acid with a hydroxyl group at the 4th position and two methyl groups at the 3rd and 5th positions. This chemical structure endows it with unique properties that make it suitable for various applications across different industries.

Uses

Used in Pharmaceutical Industry:
4-Hydroxy-3,5-dimethylbenzoic acid is used as a reagent for potent TTR amyloidogenesis inhibitors. It plays a crucial role in the development of therapeutic agents that target transthyretin (TTR) amyloidosis, a condition characterized by the abnormal accumulation of TTR protein in tissues, leading to various diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Hydroxy-3,5-dimethylbenzoic acid serves as an important intermediate in the synthesis of various compounds. Its presence in this industry is vital for the development of new and improved agrochemical products, such as pesticides and herbicides, which are essential for maintaining agricultural productivity and crop protection.
Used in Dye Industry:
4-Hydroxy-3,5-dimethylbenzoic acid is also utilized in the dye industry as an intermediate for the production of various dyestuffs. Its unique chemical properties contribute to the development of new and innovative dyes with enhanced color properties and improved performance characteristics.
Used in Chemical Synthesis:
4-Hydroxy-3,5-dimethylbenzoic acid is used in the preparation of mexiletine derivatives. Mexiletine is an antiarrhythmic drug used to treat abnormal heart rhythms. The synthesis of mexiletine derivatives involves the use of 4-Hydroxy-3,5-dimethylbenzoic acid as a key intermediate, highlighting its importance in the pharmaceutical sector.

Check Digit Verification of cas no

The CAS Registry Mumber 4919-37-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4919-37:
(6*4)+(5*9)+(4*1)+(3*9)+(2*3)+(1*7)=113
113 % 10 = 3
So 4919-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c1-5-3-7(9(11)12)4-6(2)8(5)10/h3-4,10H,1-2H3,(H,11,12)/p-1

4919-37-3 Well-known Company Product Price

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  • Alfa Aesar

  • (A13051)  4-Hydroxy-3,5-dimethylbenzoic acid, 98%   

  • 4919-37-3

  • 1g

  • 313.0CNY

  • Detail
  • Alfa Aesar

  • (A13051)  4-Hydroxy-3,5-dimethylbenzoic acid, 98%   

  • 4919-37-3

  • 5g

  • 1325.0CNY

  • Detail
  • Alfa Aesar

  • (A13051)  4-Hydroxy-3,5-dimethylbenzoic acid, 98%   

  • 4919-37-3

  • 25g

  • 5298.0CNY

  • Detail

4919-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-3,5-dimethylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-4-hydroxybenzoic 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:4919-37-3 SDS

4919-37-3Synthetic route

4-methoxy-3,5-dimethylbenzoic acid
21553-46-8

4-methoxy-3,5-dimethylbenzoic acid

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
With pyridine hydrochloride at 200℃; for 0.5h; Microwave irradiation; Ionic liquid;96%
With hydrogen bromide
3,5-dimethyl-4-benzyloxy-benzoic acid
97888-80-7

3,5-dimethyl-4-benzyloxy-benzoic acid

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
With tetrabutylammomium bromide; hydrogen bromide In dichloromethane for 24h; Heating;87.3%
methanol
67-56-1

methanol

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
at 40 - 60℃; Microwave irradiation;85%
carbon monoxide
201230-82-2

carbon monoxide

4-iodo-2,6-dimethylphenol
10570-67-9

4-iodo-2,6-dimethylphenol

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
With water; potassium carbonate at 100℃; for 24h;79%
carbon dioxide
124-38-9

carbon dioxide

4-iodo-2,6-dimethylphenol
10570-67-9

4-iodo-2,6-dimethylphenol

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
Stage #1: 4-iodo-2,6-dimethylphenol With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.333333h;
Stage #2: carbon dioxide In tetrahydrofuran; hexane at -78℃; for 0.5h;
41%
2.6-dimethylphenol
576-26-1

2.6-dimethylphenol

carbon dioxide
124-38-9

carbon dioxide

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
Stage #1: 2.6-dimethylphenol With sodium hydride
Stage #2: carbon dioxide Kolbe-Schmidt reaction;
34%
(i) NaOMe, (ii) /BRN= 1900390/; Multistep reaction;
Mesitol
527-60-6

Mesitol

A

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

B

3,5-dimethylsalicylic acid
6245-04-1

3,5-dimethylsalicylic acid

Conditions
ConditionsYield
With potassium carbonate beim Schmelzen;
4-hydroxy-3,5-dimethylbenzaldehyde
2233-18-3

4-hydroxy-3,5-dimethylbenzaldehyde

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
With sodium hydroxide; silver(l) oxide
4-amino-3,5-dimethylbenzoic acid
4919-40-8

4-amino-3,5-dimethylbenzoic acid

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
With potassium nitrite; sulfuric acid
With copper(II) sulfate Diazotization;
Mesitol
527-60-6

Mesitol

potassium hydroxide

potassium hydroxide

A

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

B

3,5-dimethylsalicylic acid
6245-04-1

3,5-dimethylsalicylic acid

Conditions
ConditionsYield
beim Schmelzen;
4-hydroxy-3,5-dimethylbenzaldehyde
2233-18-3

4-hydroxy-3,5-dimethylbenzaldehyde

potash

potash

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
beim Schmelzen;
3.5-dimethyl-benzoic acid sulfamide-(4)

3.5-dimethyl-benzoic acid sulfamide-(4)

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
With potassium carbonate beim Schmelzen;
With sodium hydroxide beim Schmelzen;
carbon dioxide
124-38-9

carbon dioxide

sodium 2,6-dimethylphenolate
16081-16-6

sodium 2,6-dimethylphenolate

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

4-amino-3,5-dimethylbenzoic acid
4919-40-8

4-amino-3,5-dimethylbenzoic acid

cis-nitrous acid
7782-77-6

cis-nitrous acid

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

4-oxy-3.5-dimethyl-benzaldehyde

4-oxy-3.5-dimethyl-benzaldehyde

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
With potassium hydroxide
3,5-dimethyl-4-hydroxybenzonitrile
4198-90-7

3,5-dimethyl-4-hydroxybenzonitrile

KOH

KOH

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
beim Schmelzen;
3,5-dimethyl-4-sulfamoyl-benzoic acid

3,5-dimethyl-4-sulfamoyl-benzoic acid

potassium hydroxide

potassium hydroxide

3,5-dimethyl-4-hydroxybenzoic acid
4919-37-3

3,5-dimethyl-4-hydroxybenzoic acid

Conditions
ConditionsYield
gelindes Schmelzen;

4919-37-3Relevant articles and documents

New secondary metabolites from Allium victorialis

Khan, Sadia,Fatima, Itrat,Hussain Kazmi, Mehdi,Malik, Abdul

, p. 1176 - 1181 (2013)

Allumines A and B (1 and 2, resp.), two new steroidal alkaloids, and a new cyclopentene derivative, 3, were isolated from the CHCl3-soluble fraction of the whole plant of Allium victorialis. Their structures were elucidated by spectroscopic techniques, including 1D- and 2D-NMR spectroscopy. Copyright

Preparation method of propofol and structural analogues of propofol

-

Paragraph 0074-0080, (2017/08/28)

The invention relates to a preparation method of propofol and structural analogues of propofol. The preparation method comprises the steps as follows: preparing an intermediate from p-hydroxybenzoic acid and alkyl alcohol as raw materials under the action of a solid acid catalyst, and then preparing a target product by a decarboxylase reaction. The preparation method has the characteristics of being green in synthesis, realizing biotransformation, causing little pollution, producing few by-products and the like, and is suitable for industrial production; the purity of the prepared products such as propofol is 99.6% or higher, which meets various medicinal standards.

Facile cleavage of ethers in ionic liquid

Cheng, Lili,Aw, Carlin,Ong, Siew Siang,Lu, Yixin

supporting information; experimental part, p. 2008 - 2010 (2009/08/14)

Various alkyl ethers were efficiently cleaved by treating them with pyridinium halides in ionic liquid, and the desired products were obtained in excellent yields.

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