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1-(4-nitrophenyl)-3-(pyrrolidin-1-yl)propan-1-one hydrochloride (1:1) is a chemical compound with the molecular formula C15H18ClNO3. It is a derivative of 1-(4-nitrophenyl)-3-(pyrrolidin-1-yl)propan-1-one, where a hydrochloric acid molecule is associated with the compound in a 1:1 ratio. This association results in the formation of a salt, which is a common method to improve the solubility and stability of certain organic compounds. The compound is characterized by the presence of a 4-nitrophenyl group, a pyrrolidin-1-yl group, and a propan-1-one moiety. It is used in various chemical and pharmaceutical applications, particularly in the synthesis of drugs and other bioactive molecules.

6287-76-9

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6287-76-9 Usage

Uses

Used in Biochemical and Pharmaceutical Research:
1-(4-nitrophenyl)-3-(pyrrolidin-1-yl)propan-1-one hydrochloride (1:1) is used as a reagent for [facilitating biochemical reactions and pharmaceutical drug synthesis] due to its ability to interact with biological molecules and its role in the synthesis of various organic compounds.
Used in Analytical Chemistry:
In the field of Analytical Chemistry, 1-(4-nitrophenyl)-3-(pyrrolidin-1-yl)propan-1-one hydrochloride (1:1) is used as a standard reference material for [ensuring accuracy and consistency in experimental results] because of its well-defined chemical properties and strong binding affinity with specific biological molecules.
Used in Synthesis of Organic Compounds:
1-(4-nitrophenyl)-3-(pyrrolidin-1-yl)propan-1-one hydrochloride (1:1) is used as a precursor in the synthesis of various organic compounds for [enabling the creation of diverse chemical structures] that can be applied in different industries, such as pharmaceuticals, materials science, and agrochemicals.
Used in Medical Research:
In the medical field, 1-(4-nitrophenyl)-3-(pyrrolidin-1-yl)propan-1-one hydrochloride (1:1) is studied for its potential therapeutic applications in [various medical conditions] due to its strong binding affinity with certain biological molecules, which may lead to the development of new treatments or therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 6287-76-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6287-76:
(6*6)+(5*2)+(4*8)+(3*7)+(2*7)+(1*6)=119
119 % 10 = 9
So 6287-76-9 is a valid CAS Registry Number.

6287-76-9SDS

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 1-(4-nitrophenyl)-3-pyrrolidin-1-ylpropan-1-one,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:6287-76-9 SDS

6287-76-9Downstream Products

6287-76-9Relevant academic research and scientific papers

Dramatically accelerated synthesis of β-aminoketones via aqueous Mannich reaction under combined microwave and ultrasound irradiation

Peng, Yanqing,Dou, Ruiling,Song, Gonghua,Jiang, Jun

, p. 2245 - 2247 (2007/10/03)

An efficient green chemistry approach to the synthesis of β-aminoketones was developed under combined microwave and ultrasound irradiation. With this technique, the title compounds were rapidly synthesized in aqueous media with good yields. Georg Thieme Verlag Stuttgart.

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