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402470-91-1

N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide, also known as Zolpidem intermediate, is an organic compound that serves as a crucial reactant in the synthesis of Zolpidem. It is characterized by its molecular structure, which includes a 4-oxo-4-(p-tolyl)butanamide backbone with two methyl groups attached to the nitrogen atom. N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide plays a significant role in the pharmaceutical industry due to its involvement in the production of a widely used medication.

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  • 402470-91-1 Structure

  • Basic information

    1. Product Name: N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide
    2. Synonyms: N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide;Zolpidem Related Compound 1;N,N-Dimethyl-3-(4-methylbenzoyl)propionamide
    3. CAS NO:402470-91-1
    4. Molecular Formula: C13H17NO2
    5. Molecular Weight: 219.27958
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 402470-91-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide(402470-91-1)
    11. EPA Substance Registry System: N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide(402470-91-1)

  • 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: 402470-91-1(Hazardous Substances Data)

402470-91-1 Usage

Uses

Used in Pharmaceutical Industry:
N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide is used as a reactant for the synthesis of Zolpidem, which is a medication primarily prescribed for the short-term treatment of insomnia. It helps in addressing sleep disorders by inducing sleep and improving sleep quality in patients who have difficulty falling asleep or staying asleep.
N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide's role in the synthesis of Zolpidem highlights its importance in the development of effective treatments for insomnia, a condition that affects millions of people worldwide. By facilitating the production of Zolpidem, N,N-DiMethyl-4-oxo-4-(p-tolyl)butanaMide contributes to the improvement of sleep health and overall well-being for those suffering from sleep-related issues.

Check Digit Verification of cas no

The CAS Registry Mumber 402470-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,4,7 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 402470-91:
(8*4)+(7*0)+(6*2)+(5*4)+(4*7)+(3*0)+(2*9)+(1*1)=111
111 % 10 = 1
So 402470-91-1 is a valid CAS Registry Number.

402470-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethyl-4-oxo-4-(p-tolyl)butanamide

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-4-(4-methylphenyl)-4-oxobutanamide

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:402470-91-1 SDS

402470-91-1Relevant articles and documents

A from the aromatic acid directly preparing aromatic ketone method (by machine translation)

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Paragraph 0195; 0196, (2019/01/06)

A process for preparing aryl ketone of the method, it is in order to aromatic carboxylic acid (ArCOOH) and olefin as raw materials, triphenylphosphine as a deoxidizing agent, under the irradiation of the blue lamp, in dichloromethane and water solution, under argon atmosphere, in the presence of a small amount of potassium phosphate, in order to [Ir (dF (CF3 ) Ppy)2 (Dtbbpy)] PF6 As the photocatalyst, get the aromatic compounds. The method easily available raw materials, mild reaction conditions, wide adaptability. (by machine translation)

Tributylphosphine-catalyzed Stetter reaction of N,N-dimethylacrylamide: Synthesis of N,N-dimethyl-3-aroylpropionamides

Gong, Ji Hyeon,Im, Yang Jin,Lee, Ka Young,Kim, Jae Nyoung

, p. 1247 - 1251 (2007/10/03)

The reaction of arylaldehydes 1 and N,N-dimethylacrylamide in the presence of tributylphosphine afforded N,N-dimethyl-3-aroylpropionamides 2 in moderate yields. The reaction might involve the formation of α-oxo ylide A.

Chemistry, Binding Affinities, and Behavioral Properties of a New Class of "Antineophobic" Mitochondrial DBI Receptor Complex (mDRC) Ligands

Kozikowski, A. P.,Ma, D.,Brewer, James,Sun, S.,Costa, E.,et al.

, p. 2908 - 2920 (2007/10/02)

The mitochondrial DBI receptor complex (mDRC; previously called the peripheral benzodiazepine receptors) is linked to the production of neurosteroids such as pregnenolone sulfate, dehydroepiandrosterone sulfate, and others.In order to gain further informa

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