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2,4-Pentanedione, 3-(1-aminoethylidene)(9CI), also known as 3-amino-1-phenylbutan-1-one, is a chemical compound with the molecular formula C7H11NO. It is a derivative of pentanedione and exhibits a pale yellow liquid appearance with a fruity odor. 2,4-Pentanedione, 3-(1-aminoethylidene)(9CI) is soluble in most organic solvents and is commonly used as a reagent in organic chemical synthesis and pharmaceutical research and development. Due to its potential to cause irritation to the skin, eyes, and respiratory system, as well as allergic reactions in some individuals, careful handling is advised.

73845-28-0

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73845-28-0 Usage

Uses

Used in Organic Chemical Synthesis:
2,4-Pentanedione, 3-(1-aminoethylidene)(9CI) is used as a reagent in organic chemical synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, 2,4-Pentanedione, 3-(1-aminoethylidene)(9CI) serves as a valuable compound in research and development. Its unique structure allows it to be utilized in the creation and modification of pharmaceutical agents, potentially leading to the discovery of new drugs and therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 73845-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,4 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73845-28:
(7*7)+(6*3)+(5*8)+(4*4)+(3*5)+(2*2)+(1*8)=150
150 % 10 = 0
So 73845-28-0 is a valid CAS Registry Number.

73845-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-aminoethylidene)pentane-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-(1-AMINOETHYLIDENE)-2,4-PENTANEDIONE

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:73845-28-0 SDS

73845-28-0Downstream Products

73845-28-0Relevant academic research and scientific papers

CYCLIC DIARYLBORON DERIVATIVES AS NLRP3 INFLAMMASOME INHIBITORS

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Paragraph 00159, (2017/02/24)

Inhibitor compounds are disclosed. The compounds are effective in the treatment of diseases or conditions in which interleukin 1 β activity is implicated. Methods of synthesis of the compounds, as well as pharmaceutical compositions comprising the compounds are also disclosed.

Reactions of β-diketone compounds with nitriles catalyzed by Lewis acids: A simple approach to β-enaminone synthesis

Cheng, Xu,Pei, Shuchen,Xue, Chenchen,Cao, Kaifei,Hai, Li,Wu, Yong

, p. 63897 - 63900 (2015/02/19)

Aluminium chloride selectively promoted the nucleophilic attack of β-diketone compounds with nitriles to give enaminones. Moreover a plausible mechanism for this transformation was given.

Chemistry of hexamethyldisilazane. Silylation of β-diketones and amination of β-triketones

Chu, Daniel T. W.,Huckin, Stuart N.

, p. 138 - 142 (2007/10/02)

It is discovered that hexamethyldisilazane, a reagent generally used to silylate amino, hydroxyl, sulfhydryl, and carbonyl groups, reacts with β-diketones to form their trimethylsilyl enol ethers in high yield.An efficient and simple procedure for aminati

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