Noun:

আমি খনি,

imine's Usage Examples:

An imine (/ɪˈmiːn/ or /ˈɪmɪn/) is a functional group or chemical compound containing a carbon–nitrogen double bond.

Aziridine Systematic IUPAC name Azacyclopropane Other names Azirane Ethylene imine Aminoethylene Dimethyleneimine Dimethylenimine Ethylimine Identifiers CAS.

alkylimino-de-oxo-bisubstitution, to form the imine.

The equilibrium between aldehyde/ketone and imine can be shifted toward imine formation by removal of the formed.

NAPQI, also known as NAPBQI or N-acetyl-p-benzoquinone imine, is a toxic byproduct produced during the xenobiotic metabolism of the analgesic paracetamol.

tautomeric form of an imine.

This usually will rearrange to the imine; however there are several exceptions (such as aniline).

The enamine-imine tautomerism may.

Primary amines react with ketones and aldehydes to form imines.

They are the imine derivatives of amides (RC(O)NR2).

a derivative of imines formed by a condensation reaction between a ketone or aldehyde and semicarbazide.

They are classified as imine derivatives because.

An oxime is a chemical compound belonging to the imines, with the general formula RR'C=NOH, where R is an organic side-chain and R' may be hydrogen, forming.

Azetidine Systematic IUPAC name Azacyclobutane Other names Azetane Trimethylene imine 1,3-Propylenimine Identifiers CAS Number 503-29-7 Y 3D model (JSmol) Interactive.

The imine tautomer is dominant, at least in the solid state.

Molecules containing carbon—hetero double bonds like carbonyl (C=O) groups, or imine (C=N) groups, can undergo addition, as they too have double-bond character.

A ketenimine is a cumulated alkene and imine and is related to an allene and a ketene.

The parent compound is ketenimine.

N-Sulfinyl imines (N-sulfinylimines, sulfinimines, thiooxime S-oxides) are a class of imines bearing a sulfinyl group attached to nitrogen.

These imines display.

The imine Diels–Alder reaction involves the transformation of all-carbon dienes and imine dienophiles into tetrahydropyridines.

In chemistry, an imino acid is any molecule that contains both imine (>C=NH) and carboxyl (-C(=O)-OH) functional groups.

different amines the reaction becomes an exchange reaction where the two imine derivatives compete in equilibrium.

Polyethylenimine (PEI) or polyaziridine is a polymer with repeating unit composed of the amine group and two carbon aliphatic CH2CH2 spacer.

Linear polyethyleneimines.

The amine group of tyrosine attacks the alpha carbon of the imine bonded to Lys280, forming a tetrahedral complex and then kicking off the.

Ethanimine is an organonitrogen compound classified as an imine.