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3,4,5-Trimethoxybenzamide, with the molecular formula C10H13NO4, is an amide derivative of 3,4,5-trimethoxybenzoic acid. It is a white to off-white crystalline powder with a melting point of 119-121°C and is soluble in organic solvents. This chemical compound primarily serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and is also utilized in the production of dyes, pigments, and other specialty chemicals.

3086-62-2

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3086-62-2 Usage

Uses

Used in Pharmaceutical Industry:
3,4,5-Trimethoxybenzamide is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical industry, 3,4,5-Trimethoxybenzamide is employed as an intermediate in the production of various agrochemicals, contributing to the development of effective and safe products for agricultural applications.
Used in Dye and Pigment Production:
3,4,5-Trimethoxybenzamide is used as a key component in the manufacturing process of dyes and pigments, providing a wide range of color options and enhancing the performance of these products.
Used in Specialty Chemicals:
3,4,5-TRIMETHOXYBENZAMIDE is also utilized in the production of specialty chemicals, where its unique properties contribute to the development of innovative and high-quality products for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3086-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3086-62:
(6*3)+(5*0)+(4*8)+(3*6)+(2*6)+(1*2)=82
82 % 10 = 2
So 3086-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO4/c1-13-7-4-6(10(11)12)5-8(14-2)9(7)15-3/h4-5H,1-3H3,(H2,11,12)

3086-62-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L12155)  3,4,5-Trimethoxybenzamide, 98%   

  • 3086-62-2

  • 25g

  • 533.0CNY

  • Detail
  • Alfa Aesar

  • (L12155)  3,4,5-Trimethoxybenzamide, 98%   

  • 3086-62-2

  • 100g

  • 1728.0CNY

  • Detail

3086-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5-TRIMETHOXYBENZAMIDE

1.2 Other means of identification

Product number -
Other names 3,5-Trimethoxybenzamide

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:3086-62-2 SDS

3086-62-2Relevant academic research and scientific papers

Photophysical properties and photoreduction of N-acetyl- and N-benzoylphthalimides

Biczók, László,G?rner, Helmut

, p. 10 - 15 (2012)

The photophysical properties and photoreduction of N-acetylphthalimide (AcP) and N-benzoylphthalimide (BzP), N-3,4,5-trimethoxybenzoylphthalimide (trimethoxyBzP) and N-4-nitrobenzoylphthalimide (nitroBzP) were studied by steady-state and transient techniques. Radicals and their precursor triplet states were detected by flash photolysis. The triplet state properties of AcP and BzP were characterized. In contrast, no triplet absorption was observed with ns-detection for trimethoxyBzP and nitroBzP. Specific products are formed upon electron transfer from triethylamine to the photoexcited acylphthalimides. In addition, H-atom transfer from 2-propanol or other alcohols to the triplet state takes place. The properties of several radical intermediates involved in photoreduction of the acylphthalimides as well as some structure-function relationships are described.

Single-pot tandem oxidative/C-H modification amidation process using ultrasmall PdNP-encapsulated porous organosilica nanotubes

Gholipour, Behnam,Liu, Xiao,Rostamnia, Sadegh,Zonouzi, Afsaneh

, p. 4276 - 4287 (2022/02/16)

Herein, we studied a single-pot method with a dual catalysis process towards the conversion of primary aromatic alcohols to amides using ultrasmall PdNPs of controlled uniform size (1.8 nm) inside hybrid mesoporous organosilica nanotubes (MO-NTs). The cat

Nano-construction of CuO nanorods decorated with g-C3N4 nanosheets (CuO/g-C3N4-NS) as a superb colloidal nanocatalyst for liquid phase C[sbnd]H conversion of aldehydes to amides

Mohammadi, Robabeh,Gholipour, Behnam,Alamgholiloo, Hassan,Rostamnia, Sadegh,Mohtasham, Hamed,Zonouzi, Afsaneh,Ramakrishna, Seeram,Shokouhimehr, Mohammadreza

, (2021/04/27)

Herein, we describe an intelligent strategy to fabricate nanosheets of graphitic carbon nitride (g-C3N4) decorated with nanorods copper oxide (CuO NRs). Then, the catalytic activity of CuONRs/g-C3N4-NS was developed for the synthesis of primary amides in water. The morphology of CuO and its synergetics effect with nanosheets g-C3N4 a major role in the yield of products. Furthermore, hydroxylamine hydrochloride (NH2OH·HCl) due to availability and affordability was used as a suitable substitute for ammonia source. The findings demonstrate that this layer nanostructure is a superb catalyst for converting various derivatives of aldehyde to their corresponding amides. The current protocol can be useful criterion in the synthesis and stabilization of metal oxides and provides new insight in organic transformation.

Chemoselective Synthesis of Aryl Ketones from Amides and Grignard Reagents via C(O)-N Bond Cleavage under Catalyst-Free Conditions

Sureshbabu, Popuri,Azeez, Sadaf,Muniyappan, Nalluchamy,Sabiah, Shahulhameed,Kandasamy, Jeyakumar

, p. 11823 - 11838 (2019/10/02)

Conversion of a wide range of N-Boc amides to aryl ketones was achieved with Grignard reagents via chemoselective C(O)-N bond cleavage. The reactions proceeded under catalyst-free conditions with different aryl, alkyl, and alkynyl Grignard reagents. α-Ketoamide was successfully converted to aryl diketones, while α,β-unsaturated amide underwent 1,4-addition followed by C(O)-N bond cleavage to provide diaryl propiophenones. N-Boc amides displayed higher reactivity than Weinreb amides with Grignard reagents. A broad substrate scope, excellent yields, and quick conversion are important features of this methodology.

Base promoted peroxide systems for the efficient synthesis of nitroarenes and benzamides

Gupta, Sampa,Ansari, Alisha,Sashidhara, Koneni V.

supporting information, (2019/09/07)

A useful and efficient approach for the synthesis of nitroarenes from several aromatic amines (including heterocycles) using peroxide and base has been developed. This oxidative reaction is very easy to handle and afforded the products in good yields. Formation of benzamides from benzylamine was also successfully carried out with this metal-free catalytic system in good to excellent yields.

Uniformly dispersed copper nanoparticles onto the modified magnetically recoverable nanocatalyst for aqueous synthesis of primary amides

Ziaee, Fariborz,Gholizadeh, Mostafa,Seyedi, Seyed Mohammad

, (2017/09/06)

Magnetically recoverable and environmentally friendly Cu-based heterogeneous catalyst has been synthesized for the one-pot conversion of aldehydes to their corresponding primary amides. The Fe3O4@SiO2 nanocomposites were prepared by synthesis of Fe3O4 magnetic nanoparticles (MNPs) which was then coated with a silica shell via St?ber method. Bi-functional cysteine amino acid was covalently bonded onto the siliceous shell of nanocatalyst. The CuII ions were then loaded onto the modified surface of nanocatalyst. Finally, uniformly dispersed copper nanoparticles were achieved by reduction of CuII ions with NaBH4. Amidation reaction of aryl halides with electron-withdrawing or electron-donating groups and hydroxylamine hydrochloride catalyzed with Fe3O4@SiO2@Cysteine-copper (FSC-Cu) MNPs in aqueous condition gave an excellent yield of products. The FSC-Cu MNPs could be easily isolated from the reaction mixture with an external magnet and reused at least 8 times without significant loss in activity.

Metal-Free Thermal Activation of Molecular Oxygen Enabled Direct α-CH2-Oxygenation of Free Amines

Ghosh, Santanu,Jana, Chandan K.

, p. 260 - 266 (2018/02/19)

Direct oxidation of α-CH2 group of free amines is hard to achieve due to the higher reactivity of amine moiety. Therefore, oxidation of amines involves the use of sophisticated metallic reagents/catalyst in the presence or absence of hazardous oxidants under sensitive reaction conditions. A novel method for direct C-H oxygenation of aliphatic amines through a metal-free activation of molecular oxygen has been developed. Both activated and unactivated free amines were oxygenated efficiently to provide a wide variety of amides (primary, secondary) and lactams under operationally simple conditions without the aid of metallic reagents and toxic oxidants. The method has been applied to the synthesis of highly functionalized amide-containing medicinal drugs, such as O-Me-alibendol and -buclosamide.

A selective hydration of nitriles catalysed by a Pd(OAc)2-based system in water

Sanz Sharley, Daniel D.,Williams, Jonathan M.J.

supporting information, p. 4090 - 4093 (2017/09/27)

In situ formation of a [Pd(OAc)2bipy] (bipy = 2,2′-bipyridyl) complex in water selectively catalyses the hydration of a wide range of organonitriles at 70 °C. Catalyst loadings of 5 mol% afford primary amide products in excellent yields in the absence of hydration-promoting additives such as oximes and hydroxylamines.

Copper(II) acetate-catalysed conversion of aldoximes to amides under mild conditions

Ma, Xiaoyun,Lu, Ming

, p. 594 - 596 (2016/10/21)

A mild method for the metal-catalysed conversion of aldoximes to amides has been achieved by the combined use of copper(II) acetate and MeCN in EtOH under reflux. The presence of a catalytic amount of MeCN (0.05 equiv.) accelerated the reaction and improved the yield. Aryl, heteroaryl and alkyl aldoximes were transformed into the corresponding amides in moderate to good yield. 2-Furyl and 2-Thiophenyl aldoximes, which possess a heteroatom lone pair positioned ortho to the oximido group, showed enhanced reactivity, and the corresponding amides were obtained in excellent yield.

Exfoliation effect of PEG-type surfactant on Pd supported GO (SE-Pd(nanoparticle)/GO) in cascade synthesis of amides: A comparison with Pd(nanoparticle)/rGO

Rostamnia, Sadegh,Doustkhah, Esmail,Zeynizadeh, Behzad

, p. 88 - 95 (2016/04/01)

In the presence investigation, a cascade method for the synthesis of primary amides is discussed by the catalysis of Pd supported onto graphene oxide (Pd/GO) nanosheets. Also, the effect of different polyethyleneglycol-type (PEG-type) polyethers including PEG-300, P123 and F127 on the catalytic activity of Pd/rGO is studied in the the reaction of aldehyde and hydroxylamine hydrochloride to give benzamide. Addition of PEG-type polyethers played an important role in raising the catalytic power of Pd(nanoparticle)/GO by exfoliation of GO sheets. The present paper introduces Pd(nanoparticle)/GO as first Pd supported GO for the synthesis of primary amides through this method. This catalyst was highly active, efficient, tolerant, and environmentally benign in one-pot conditions with recyclability at least for 8 runs. Also, this study suggests the prevailing catalytic activity of Pd(nanoparticle)/GO rather to Pd(nanoparticle)/rGO in a comparitive experiment.

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