Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Acetamide, N-methyl-N-(2-methylphenyl)-, also known as N-Benzyl-N-methylacetamide, is an organic compound with the molecular formula C10H13NO. It is a derivative of acetamide, featuring a methyl group and a benzyl group attached to the nitrogen atom. Acetamide, N-methyl-N-(2-methylphenyl)is characterized by its potential applications in various chemical and pharmaceutical processes due to its unique structural properties.

29823-47-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 29823-47-0 Structure
  • Basic information

    1. Product Name: Acetamide, N-methyl-N-(2-methylphenyl)-
    2. Synonyms: Acetamide, N-methyl-N-(2-methylphenyl)-;N-Benzyl-N-methylacetamide
    3. CAS NO:29823-47-0
    4. Molecular Formula: C10H13NO
    5. Molecular Weight: 163.21632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29823-47-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetamide, N-methyl-N-(2-methylphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-methyl-N-(2-methylphenyl)-(29823-47-0)
    11. EPA Substance Registry System: Acetamide, N-methyl-N-(2-methylphenyl)-(29823-47-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 29823-47-0(Hazardous Substances Data)

29823-47-0 Usage

Uses

Used in Pharmaceutical Industry:
Acetamide, N-methyl-N-(2-methylphenyl)is used as a reagent for the synthesis of arylaminopyrazole derivatives. These derivatives are known as 11β-HSD1 inhibitors, which play a crucial role in the treatment of various metabolic and inflammatory disorders. Acetamide, N-methyl-N-(2-methylphenyl)-'s ability to form arylaminopyrazole derivatives makes it a valuable component in the development of novel therapeutic agents.
Used in Chemical Synthesis:
In the field of organic chemistry, Acetamide, N-methyl-N-(2-methylphenyl)serves as an intermediate for the synthesis of various complex molecules. Its unique structure allows for further functionalization and modification, making it a versatile building block for the creation of new compounds with potential applications in various industries.

Synthesis Reference(s)

Tetrahedron Letters, 14, p. 2475, 1973 DOI: 10.1016/S0040-4039(01)96182-9

Check Digit Verification of cas no

The CAS Registry Mumber 29823-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,2 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29823-47:
(7*2)+(6*9)+(5*8)+(4*2)+(3*3)+(2*4)+(1*7)=140
140 % 10 = 0
So 29823-47-0 is a valid CAS Registry Number.

29823-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ac-pm-Me

1.2 Other means of identification

Product number -
Other names N-acetyl-N-methylbenzylamine

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:29823-47-0 SDS

29823-47-0Relevant articles and documents

Preparation of alkylated compounds using the trialkylphosphate

-

Paragraph 0184-0185; 0205, (2021/11/02)

[Problem] trialkylphosphate strong base used reaction agent, a carboxylic acid, a ketone, an aldehyde, amine, amide, thiol, ester or Grignard reagent to a variety of substrates, and/or high efficiency to generate a highly stereoselective alkylation reaction, the alkylated compounds capable of producing new means. [Solution] was used as the alkylating agent in the alkylation of compound trialkylphosphate, strongly basic reaction production use. [Drawing] no

Regio- And Stereoselective (S N2) N -, O -, C - And S -Alkylation Using Trialkyl Phosphates

Banerjee, Amit,Hattori, Tomohiro,Yamamoto, Hisashi

, (2021/06/16)

Bimolecular nucleophilic substitution (S N 2) is one of the most well-known fundamental reactions in organic chemistry to generate new molecules from two molecules. In principle, a nucleophile attacks from the back side of an alkylating agent having a suitable leaving group, most commonly a halide. However, alkyl halides are expensive, very harmful, toxic and not so stable, which makes them problematic for laboratory use. In contrast, trialkyl phosphates are inexpensive, readily accessible and stable at room temperature, under air, and are easy to handle, but rarely used as alkylating agents in organic synthesis. Here, we describe a mild, straightforward and powerful method for nucleophilic alkylation of various N -, O -, C - and S -nucleophiles using readily available trialkyl phosphates. The reaction proceeds smoothly in excellent yield, and quantitative yield in many cases, and covers a wide range of substrates. Further, the rare stereoselective transfer of secondary alkyl groups has been achieved with inversion of configuration of chiral centers (up to 98% ee).

RuO4-mediated oxidation of tertiary amines. stereoelectronic effects

Petride, Horia,Florea, Cristina,H?rtopeanu, Anca,Stavarache, Cristina

, p. 89 - 96 (2021/02/05)

Tertiary amines like PhCH2-NMe-CH2R (R = H, Me, CN) underwent RuO4-mediated oxidation by attack at all three N-α-positions. The various reaction products were classified in three groups, according to the functionalized sit

COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY

-

Page/Page column 478; 479, (2019/02/13)

In one aspect, compounds of Formula AA, or a pharmaceutically acceptable salt thereof, are featured.The variables shown in Formula AA are as defined in the claims. The compounds of formula AA are NLRP3 activity modulators and, as such, can be used in the treatment of metabolic disorders (e.g. Type 2 diabetes, atherosclerosis, obesity or gout), a disease of the central nervous system (e.g. Alzheimer's disease, multiple sclerosis, Amyotrophic Lateral Sclerosis or Parkinson's disease), lung disease (e.g. asthma, COPD or pulmonary idiopathic fibrosis), liver disease (e.g. NASH syndrome, viral hepatitis or cirrhosis), pancreatic disease (e.g. acute pancreatitis or chronic pancreatitis), kidney disease (e.g. acute kidney injury or chronic kidney injury), intestinal disease (e.g. Crohn's disease or Ulcerative Colitis), skin disease (e.g. psoriasis), musculoskeletal disease (e.g. scleroderma), a vessel disorder (e.g. giant cell arteritis), a disorder of the bones (e.g. osteoarthritis, osteoporosis or osteopetrosis disorders), eye disease (e.g. glaucoma or macular degeneration), a disease caused by viral infection (e.g. HIV or AIDS), an autoimmune disease (e.g. Rheumatoid Arthritis, Systemic Lupus Erythematosus or Autoimmune Thyroiditis), cancer or aging.

Amide Bond Formation Catalyzed by Recyclable Copper Nanoparticles Supported on Zeolite Y under Mild Conditions

Moglie, Yanina,Buxaderas, Eduardo,Mancini, Agustina,Alonso, Francisco,Radivoy, Gabriel

, p. 1487 - 1494 (2019/02/16)

A series of catalysts based on supported copper nanoparticles have been prepared and tested in the amide bond formation from tertiary amines and acid anhydrides, in the presence of tert-butyl hydroperoxide as an oxidant. Copper nanoparticles on zeolite Y (CuNPs/ZY) was found to be the most efficient catalyst for the synthesis of amides, working in acetonitrile as solvent, under ligand- and base-free conditions in air. The products were obtained in good to excellent yields and in short reaction times. The CuNPs/ZY system also exhibited higher catalytic activity than some commercially available copper and iron sources and it was reused in ten reaction cycles without any further pre-treatment. This methodology has been successfully scaled-up to a gram scale with no detriment to the yield.

Direct Reductive N-Functionalization of Aliphatic Nitro Compounds

Rauser, Marian,Ascheberg, Christoph,Niggemann, Meike

supporting information, p. 3970 - 3974 (2018/02/26)

The first general protocol for the direct reductive N-functionalization of aliphatic nitro compounds is presented. The nitro group is partially reduced to a nitrenoid, with a mild and readily available combination of B2pin2 and zinc organyls. Thereby, the formation of an unstable nitroso intermediate is avoided, which has so far severely limited reductive transformations of aliphatic nitro compounds. The reaction is concluded by an electrophilic amination of zinc organyls.

Diphenylsilane as a coupling reagent for amide bond formation

Sayes, Morgane,Charette, André B.

supporting information, p. 5060 - 5064 (2017/11/09)

A simple procedure for amide bond formation using diphenylsilane as a coupling reagent is described. This methodology enables the direct coupling of carboxylic acids with primary and secondary amines, releasing only hydrogen and a siloxane as by-products. Only one equivalent of each partner is needed, providing a more sustainable amidation method producing minimal wastes. This methodology was also extended to the synthesis of peptides and lactams by addition of Hünig's base (DIPEA) and 4-dimethylaminopyridine (DMAP).

Chemoselective N-acetylation of primary aliphatic amines promoted by pivalic or acetic acid using ethyl acetate as an acetyl donor

Yoshida, Tomoki,Kawamura, Shimpei,Nakata, Kenya

supporting information, p. 1181 - 1184 (2017/03/02)

The combination of pivalic or acetic acid as a promoter and EtOAc as a solvent and acetyl donor proved to be efficient for the chemoselective N-acetylation of primary aliphatic amines to afford the corresponding acetamides. We developed a simple and convenient approach, which requires mild reaction conditions. Competitive inter- and intramolecular reactions between aliphatic amines, alcohols, and aromatic amines were examined, and chemoselectivity was achieved by adjusting the conditions of the reaction.

Acetic acid as a catalyst for the N-acylation of amines using esters as the acyl source

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

supporting information, p. 2020 - 2023 (2017/02/15)

We report a cheap and simple method for the acetylation of a variety of amines using catalytic acetic acid and either ethyl acetate or butyl acetate as the acyl source. Catalyst loadings as low as 10 mol% afforded acetamide products in excellent yields at temperatures ranging from 80-120 °C. The methodology can also be successfully applied for the synthesis of a broad range of other amides, including the formation of formamides at 20 °C.

A process for preparing 4 - amino - N - alkyl benzyl amine method

-

Page/Page column 0044-0046; 0105-0107, (2017/08/26)

The present invention belongs to an organic intermediate preparation, and particularly relates to a 4-amino-N-alkyl benzylamine preparation method. According to the present invention, N-alkyl benzylamine is adopted as a raw material, acetylation, positioning nitrification and deprotection are performed, and hydrogenation reducing is performed in the presence of a multi-component skeleton Ni-Fe-Cu catalyst, wherein the total yield is more than or equal to 90%; and the method has characteristics of simple process, mild operating conditions and low pollution, the catalyst used in the reaction has high activity and high selectivity, the catalytic hydrogenation selectivity is more than or equal to 99.9%, the yield is more than or equal to 99.9%, the catalyst can be repeatedly applied, and the production cost can be effectively reduced compared with the traditional process.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 29823-47-0