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2-bromo-2-methyl-N-(4-nitrophenyl)propanamide is a chemical compound with the molecular formula C10H12BrNO3. It is a derivative of propanamide, featuring a 2-bromo-2-methyl group and a 4-nitrophenyl group attached to the nitrogen atom. 2-bromo-2-methyl-N-(4-nitrophenyl)propanamide is characterized by its bromine atom, which provides it with unique reactivity and properties. It is often used in organic synthesis and as an intermediate in the production of pharmaceuticals and other chemical products. The presence of the nitro group gives it potential applications in the synthesis of explosives and other energetic materials. Its structure and properties make it a versatile building block in the field of organic chemistry.

2322-52-3

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2322-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2322-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2322-52:
(6*2)+(5*3)+(4*2)+(3*2)+(2*5)+(1*2)=53
53 % 10 = 3
So 2322-52-3 is a valid CAS Registry Number.

2322-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2-methyl-N-(4-nitrophenyl)propanamide

1.2 Other means of identification

Product number -
Other names 2-bromo-2-methyl-p-nitropropananilide

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:2322-52-3 SDS

2322-52-3Relevant academic research and scientific papers

Bromo-nitro substitution on a tertiary α carbon - A previously uncharacterized facet of the Kornblum substitution

Leonard, Matthew J.,McKay, Peter G.,Lingham, Anthony R.

, p. 76401 - 76418 (2015/09/22)

Sodium nitrite in dimethylformamide substitutes nitro for bromine alpha to an amide carbonyl in high yield at a tertiary site. Hammett plots show a strongly positive ρ value (+0.67), indicating a negatively-charged transition state, in contrast to the typical SN1/SN2 mechanism domain for Kornblum substitutions. 2015

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