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3,5-Dihydroxybenzamide, also known as 3,5-Dihydroxybenzylamine, is a chemical compound with the molecular formula C7H7NO3. It is a derivative of benzamide and contains two hydroxyl groups on the benzene ring. 3,5-Dihydroxybenzamide possesses potential medical applications, including antiviral and anti-inflammatory properties, and is being studied for its ability to inhibit the growth of certain viruses and as a potential treatment for inflammatory diseases. It is also being investigated for its potential use in the development of new pharmaceuticals. Further research is needed to fully understand the potential uses and effects of 3,5-Dihydroxybenzamide.

3147-62-4

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3147-62-4 Usage

Uses

Used in Pharmaceutical Industry:
3,5-Dihydroxybenzamide is used as a potential antiviral agent for its ability to inhibit the growth of certain viruses, offering a new avenue for the treatment of viral infections.
3,5-Dihydroxybenzamide is used as an anti-inflammatory agent for its potential to treat inflammatory diseases, providing a novel therapeutic approach to managing inflammation-related conditions.
Used in Drug Development:
3,5-Dihydroxybenzamide is used as a compound in the development of new pharmaceuticals, leveraging its unique chemical structure and properties to create innovative treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 3147-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,4 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3147-62:
(6*3)+(5*1)+(4*4)+(3*7)+(2*6)+(1*2)=74
74 % 10 = 4
So 3147-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO3/c8-7(11)4-1-5(9)3-6(10)2-4/h1-3,9-10H,(H2,8,11)

3147-62-4 Well-known Company Product Price

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  • TCI America

  • (D2875)  3,5-Dihydroxybenzamide  >98.0%(HPLC)(N)

  • 3147-62-4

  • 5g

  • 950.00CNY

  • Detail

  • Alfa Aesar

  • (L08457)  3,5-Dihydroxybenzamide, 97%   

  • 3147-62-4

  • 1g

  • 441.0CNY

  • Detail

  • Alfa Aesar

  • (L08457)  3,5-Dihydroxybenzamide, 97%   

  • 3147-62-4

  • 5g

  • 1574.0CNY

  • Detail

3147-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Dihydroxybenzamide

1.2 Other means of identification

Product number -
Other names 3,5-Dihydroxybenzoic acid amide

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:3147-62-4 SDS

3147-62-4Downstream Products

3147-62-4Relevant academic research and scientific papers

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

Novel Enzymatic De-esterification Studies on Substituted Polyacetoxybenzamides

Parmar, Virinder S.,Kumar, Ajay,Prasad, Ashok K.,Kumar, Rajesh,Bisht, Kirpal S.,Poonam,Jain, Subhash C.,Olsen, Carl E.

, p. 810 - 822 (2007/10/03)

The regioselective capabilities of porcine pancreatic lipase in tetrahydrofuran and Candida rugosa lipase in diisopropyl ether have been investigated for selective deacetylation of peracetates of primary, secondary and tertiary amides of 2-hydroxy-, 2,4-dihydroxy-, 2,5-dihydroxy-, 3,5-dihydroxy- and 3,4,5-trihydroxybenzoic acids. The lipases exhibit random selectivity for the deacetylation of ortho-, meta- and para-acetoxy functions of di/triacetoxybenzamides leading to the formation of the corresponding partially and/or completely deacetylated benzamides. The amide group of all substrates under investigation remains inert to enzymatic hydrolysis. The results of deesterification are in good agreement with our earlier proposed mechanism of action of porcine pancreatic lipase on diaryl or aryl alkyl ketones in organic solvents.

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