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2235-46-3

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2235-46-3 Usage

Description

N,N-Diethylacetoacetamide is a β-dicarbonyl compound that exists as a clear yellow liquid. It is an important intermediate in the synthesis of various chemicals and pharmaceuticals due to its unique chemical properties.

Uses

Used in Insecticide Industry:
N,N-Diethylacetoacetamide is used as an intermediate for the manufacture of insecticides, specifically phosphamidon. Phosphamidon is an organophosphate insecticide that acts as a cholinesterase inhibitor, making it effective in controlling and eliminating insect pests.
Used in Pharmaceutical Industry:
N,N-Diethylacetoacetamide is utilized as an intermediate in the synthesis of potent calcium channel blockers. These blockers include 2,6,6-trimethyl-3-diethylaminocarbonyl-4-aryl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivatives and N,N-diethyl-2,6,6-trimethyl-4-(3-nitrophenyl)-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxamide. These compounds are essential in the treatment of various cardiovascular diseases.
Used in Chemical Synthesis:
N,N-Diethylacetoacetamide can undergo Michael addition in the presence of a bis(2,4-pentanedionato)nickel(II) catalyst. This reaction is crucial in the synthesis of various organic compounds, further expanding the utility of N,N-Diethylacetoacetamide in the chemical industry.

Flammability and Explosibility

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 2235-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2235-46:
(6*2)+(5*2)+(4*3)+(3*5)+(2*4)+(1*6)=63
63 % 10 = 3
So 2235-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO2/c1-4-9(5-2)8(11)6-7(3)10/h4-6H2,1-3H3

2235-46-3 Well-known Company Product Price

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  • Alfa Aesar

  • (B24019)  N,N-Diethylacetoacetamide, 97%   

  • 2235-46-3

  • 50g

  • 284.0CNY

  • Detail
  • Alfa Aesar

  • (B24019)  N,N-Diethylacetoacetamide, 97%   

  • 2235-46-3

  • 250g

  • 614.0CNY

  • Detail

2235-46-3SDS

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 N,N-diethyl-3-oxobutanamide

1.2 Other means of identification

Product number -
Other names N,N-Diethylacetylacetamide

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:2235-46-3 SDS

2235-46-3Relevant articles and documents

-

Horder,J.R.,Lappert,M.F.

, p. 485 - 486 (1967)

-

NEW ANALOGS AS ANDROGEN RECEPTOR AND GLUCOCORTICOID RECEPTOR MODULATORS

-

Paragraph 0194; 0196, (2019/05/16)

The present invention relates to novel dihydropyridine derivatives of formula (I): as modulators of nuclear receptors selected from androgen receptor and glucocorticoid receptor, to processes for their preparation, to pharmaceutical compositions comprising said compounds and to the use of said for manufacturing a medicament for the treatment of pathological conditions or diseases that can improve by modulation of androgen receptor and/or glucocorticoid receptor, selected from cancer, metastasizing cancers, benign prostate hyperplasia, polycystic ovary syndrome (PCOS), hair loss, hirsutism, acne, hypogonadism, muscle wasting diseases, cachexia, Cushing's syndrome, anti-psychotic drug induced weight gain, obesity, post-traumatic stress disorder and alcoholism.

O -Iodoxybenzoic Acid (IBX)-Iodine Mediated One-Pot Deacylative Sulfonylation of 1,3-Dicarbonyl Compounds: A Synthesis of β-Carbonyl Sulfones

Katrun, Praewpan,Songsichan, Teerawat,Soorukram, Darunee,Pohmakotr, Manat,Reutrakul, Vichai,Kuhakarn, Chutima

supporting information, p. 1109 - 1121 (2017/02/24)

A combination of o-iodoxybenzoic acid (IBX) and a catalytic amount of iodine is found to promote a facile one-pot deacylative sulfonylation reaction of 1,3-dicarbonyl compounds with sodium sulfinates to yield β-carbonyl sulfones. The present method provides the target products bearing a wide variety of functional groups in one step and in good yields.

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