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3-Bromo-1-methyl-2-piperidone is a brominated heterocyclic compound with the molecular formula C6H10BrNO. It is a white to off-white crystalline solid that is soluble in organic solvents and has a melting point of 60-63°C. 3-BroMo-1-Methyl-2-piperidone is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, serving as a building block for the creation of various biologically active compounds.

49785-85-5

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49785-85-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-1-methyl-2-piperidone is used as a key intermediate for the synthesis of drugs, contributing to the development of new medications with potential therapeutic benefits.
Used in Agrochemical Industry:
3-Bromo-1-methyl-2-piperidone is used as a precursor in the production of pesticides, aiding in the creation of effective solutions for pest control and crop protection.
It is important to handle 3-Bromo-1-methyl-2-piperidone with caution due to its classification as a hazardous material.

Check Digit Verification of cas no

The CAS Registry Mumber 49785-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,8 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 49785-85:
(7*4)+(6*9)+(5*7)+(4*8)+(3*5)+(2*8)+(1*5)=185
185 % 10 = 5
So 49785-85-5 is a valid CAS Registry Number.

49785-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-?Piperidinone, 3-?bromo-?1-?methyl-

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:49785-85-5 SDS

49785-85-5Relevant academic research and scientific papers

Rapid and catalyst-free α-halogenation of ketones using N-halosuccinamides in DMSO

Sreedhar,Reddy, P. Surendra,Madhavi

, p. 4149 - 4156 (2008/03/13)

α-Halogenation of various carbonyl compounds such as β-keto-esters, cyclic ketones, and lactams with N-halosuccinamides (NBS, NCS, NIS) in the presence of DMSO proceeded very smoothly to give the corresponding α-monohalogenated products in good to excellent yields with high selectivity under catalyst-free conditions. Copyright Taylor & Francis Group, LLC.

A simple and efficient method for α-bromination of carbonyl compounds using N-bromosuccinimide in the presence of silica-supported sodium hydrogen sulfate as a heterogeneous catalyst

Das, Biswanath,Venkateswarlu, Katta,Mahender, Gurram,Mahender, Ibram

, p. 3041 - 3044 (2007/10/03)

α-Bromination of carbonyl compounds (cyclic and acyclic ketones, amides and β-ketoesters) has been achieved efficiently by treatment with N-bromosuccinimide (NBS) and catalyzed by silica-supported sodium hydrogen sulfate (NaHSO4?SiO2

Chemoenzymatic enantioselective synthesis of 3-hydroxy-2-pyrrolidinones and 3-hydroxy-2-piperidinones

Kamal, Ahmed,Ramana, K. Venkata,Ramana, A. Venkata,Babu, A. Hari

, p. 2587 - 2594 (2007/10/03)

The enantioselective synthesis of 3-hydroxypyrrolidin-2-ones and 3-hydroxy piperidin-2-ones has been carried out in high enantiomeric excess employing immobilized lipase from Pseudomonas cepacia.

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