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4-BROMO-N-METHYL PIPERIDINE, with the molecular formula C6H12BrN, is a chemical compound derived from piperidine. It features a methyl group and a bromine atom attached to the piperidine ring, giving it unique structural and chemical properties. 4-BROMO-N-METHYL PIPERIDINE serves as a versatile intermediate in the synthesis of various pharmaceuticals and organic molecules, making it a valuable building block in the development of new chemical entities.

76444-51-4

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76444-51-4 Usage

Uses

Used in Pharmaceutical Industry:
4-BROMO-N-METHYL PIPERIDINE is used as a synthetic intermediate for the development of various drugs and pharmaceuticals. Its unique structure and properties contribute to the creation of new chemical entities and compounds, enhancing the therapeutic potential of medications.
Used in Organic Synthesis:
4-BROMO-N-METHYL PIPERIDINE is used as a reagent in organic synthesis and chemical reactions. It is instrumental in introducing the piperidine moiety into various organic molecules, broadening the scope of chemical reactions and the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 76444-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,4 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76444-51:
(7*7)+(6*6)+(5*4)+(4*4)+(3*4)+(2*5)+(1*1)=144
144 % 10 = 4
So 76444-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H12BrN/c1-8-4-2-6(7)3-5-8/h6H,2-5H2,1H3

76444-51-4SDS

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 4-bromo-1-methylpiperidine

1.2 Other means of identification

Product number -
Other names 4-bromo-1-methyl-piperidine

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:76444-51-4 SDS

76444-51-4Relevant academic research and scientific papers

RING INVERSION EQUILIBRIA IN 4-CHLORO-, 4-BROMO-, AND 4-METHOXY-1-ALKYLPIPERIDINES IN A NON-POLAR SOLVENT

Bailey, Judith M.,Booth, Harold,Al-Shirayda, Hatif A.R.Y.,Trimble, Mary L.

, p. 737 - 744 (2007/10/02)

The position of ring inversion equilibrium (axial Requuatorial R) in 4-R-N-alkylpiperidines (R = Cl, Br, or OMe), dissolved in CFCl3-CDCl3, has been determined by (13)C n.m.r. spectroscopy at low temperatures.In all three series, change of NH to NMe produces a marked increase in the proportion of conformation with axial R.When R is OMe, further alterations in the N-substituent from Me to Et, Pri, and CH2CF3 do not affect the equilibrium significantly, but the signifficant changes observed when R is halogen can be related to the inductive effect of the N-substituent. (13)C Chemical shifts, proportions of conformations, and conformational free energy differences are recorded for all systems studied.

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