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N-(3,4-dichlorophenyl)butanamide, also known as N-phenylbutyramide (NPB), is a chemical compound with the molecular formula C10H12Cl2O. It is a derivative of phenylbutyric acid and is commonly used as a research chemical in the study of pharmaceuticals and neurobiology. NPB is a white crystalline solid at room temperature and is moderately soluble in water.

2150-95-0

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2150-95-0 Usage

Uses

Used in Pharmaceutical Research:
N-(3,4-dichlorophenyl)butanamide is used as a research chemical for investigating its potential therapeutic effects in treating various neurological and psychiatric disorders, including anxiety, depression, and schizophrenia.
Used in Organic Synthesis:
NPB is used as a reagent in organic synthesis, contributing to the development of new chemical compounds and reactions.
Used in Pharmaceutical Production:
N-(3,4-dichlorophenyl)butanamide serves as an intermediate in the production of pharmaceuticals, playing a crucial role in the synthesis of various medications.

Check Digit Verification of cas no

The CAS Registry Mumber 2150-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2150-95:
(6*2)+(5*1)+(4*5)+(3*0)+(2*9)+(1*5)=60
60 % 10 = 0
So 2150-95-0 is a valid CAS Registry Number.

2150-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,4-dichlorophenyl)butanamide

1.2 Other means of identification

Product number -
Other names 4-Butyrylamino-1,2-dichlor-benzol

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:2150-95-0 SDS

2150-95-0Downstream Products

2150-95-0Relevant academic research and scientific papers

Reductive acylation of nitroarenes to anilides by sodium sulfite in carboxylic acids

Ghaffarzadeh, Mohammad,Akhavan, Pegah

supporting information, p. 1417 - 1419 (2016/09/28)

A facile and efficient reductive acylation of aromatic nitro compounds to corresponding anilides using a sodium sulfite-carboxylic acid system for the first time has been reported. The sodium sulfite reagent provides the colorless reductant in combination with stoichiometric amounts of carboxylic acid and enables the formation of anilides from nitroarenes without any additives in good to excellent yields with high purities and simple work-up. Furthermore, this protocol provides a novel and complementary access to some industrially important chemicals in kilogram scale under mild conditions.

A novel synthesis of N-arylamides from nitroarenes via reductive N-acylation with red phosphorus and iodine

Du, Xiaohua,Zheng, Mei,Chen, Sheng,Xu, Zhenyuan

, p. 1953 - 1955 (2008/02/08)

A series of N-arylamides and imides were synthesized via reductive N-acylation of nitroarenes with red phosphorus and carboxylic acids, catalyzed by iodine or iodides; an I /I° redox cycle was proposed to promote the reaction. Georg Thieme Verlag Stuttgart.

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