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1-[3-bromo-4-(morpholin-4-yl)phenyl]-2,5-dimethyl-1H-pyrrole-3-carbaldehyde is a complex organic compound with the molecular formula C18H20BrNO2. It features a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom, and a carbaldehyde group, indicating the presence of an aldehyde functional group. The compound also has a 3-bromo-4-(morpholin-4-yl)phenyl moiety attached to the pyrrole ring, which adds to its structural complexity. The bromine atom and morpholine group provide additional functional groups that can participate in various chemical reactions. 1-[3-bromo-4-(morpholin-4-yl)phenyl]-2,5-dimethyl-1H-pyrrole-3-carbaldehyde is likely to be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and potential reactivity.

6299-10-1

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6299-10-1 Usage

Molecular structure

The compound has a complex molecular structure consisting of a pyrrole ring, a phenyl ring, a carbaldehyde group, a bromine atom, and a morpholine group.

Pyrrole ring

The core structure of the compound is a pyrrole ring, which is a five-membered aromatic ring containing four carbon atoms and one nitrogen atom.

Carbaldehyde group

The compound has a carbaldehyde group (-CHO) attached at the 3-position of the pyrrole ring, which is an important functional group in organic chemistry.

Bromine atom

A bromine atom is present at the 3-position of the phenyl ring, which can be used for further functionalization or as a reactive site for chemical reactions.

Morpholine group

The phenyl ring has a morpholine group (a five-membered heterocyclic amine) at the 4-position, which adds further complexity to the molecule and may influence its reactivity and properties.

Methyl groups

Two methyl groups (-CH3) are present at the 2 and 5 positions of the pyrrole ring, which can affect the compound's steric properties and reactivity.

Potential applications

Due to its unique structure and functional groups, the compound may have potential applications in medicinal chemistry or organic synthesis. However, further research is necessary to fully understand its properties and potential uses.

Reactivity

The presence of the carbaldehyde group, bromine atom, and morpholine group in the molecule suggests that it may be reactive and capable of undergoing various chemical reactions, such as nucleophilic substitution, electrophilic aromatic substitution, and condensation reactions.

Stability

The compound's stability may be influenced by the presence of the aromatic pyrrole and phenyl rings, as well as the electron-donating nature of the methyl groups. However, the stability of the compound under different conditions would need to be investigated further.

Check Digit Verification of cas no

The CAS Registry Mumber 6299-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6299-10:
(6*6)+(5*2)+(4*9)+(3*9)+(2*1)+(1*0)=111
111 % 10 = 1
So 6299-10-1 is a valid CAS Registry Number.

6299-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(dimethylamino)-1,2-diphenylbutan-2-ol 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

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More Details:6299-10-1 SDS

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