Noun:

এনানসোমার,

enantiomeric শব্দের বাংলা অর্থ এর উদাহরণ:

ওয়ারফারিন এর এনানসোমার CAS-Nummer: 5543-58-8 CAS-Nummer: 5543-57-7 ।

enantiomeric's Usage Examples:

A sample of a chemical is considered enantiopure (also termed enantiomerically pure) when it has, within the limits of detection, molecules of only.

observed rotation (α) of a sample of a compound can be used to quantify the enantiomeric excess of that compound, provided that the specific rotation ([α]) for.

abundance from an enantiopure samples of the amino acid than from racemic (enantiomerically mixed) ones.

spectroscopy, in order to simultaneously determine absolute configuration and enantiomeric purity of other chiral molecules.

It can exist in either of two enantiomeric forms, (R)-aporphine and (S)-aporphine.

be a mixture of the two enantiomeric isomers of tartaric acid.

A sample with only a single enantiomer is an enantiomerically pure or enantiopure compound.

It is racemic; its biologically active enantiomeric form is levetiracetam, now marketed as an antiepileptic drug.

formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereoisomeric) products in unequal amounts.

It is a molecule having an enantiomeric dehydrohexahydroxydiphenoyl group.

stochastically distributed enantiomeric excess can be observed.

The phenomenon is different from chiral amplification, where enantiomeric excess is present from.

Starting with a low enantiomeric excess produces a product with very high enantiomeric excess.

chemical compounds exist in different isomeric forms, which have different enantiomeric structures but the same chemical formula.

The degree of selectivity is measured by the enantiomeric excess.

secondary alcohol with a high enantiomeric excess based on the major enantiomer of the alkane that was used.

Even a slight enantiomeric excess of the alkane is.

The enantiomeric purity of l-DOPA may be analyzed by determination of the optical rotation.

enantioenriched or heterochiral when its enantiomeric ratio is greater than 50:50 but less than 100:0.

Saclofen has two enantiomeric forms.

This enantiomeric excess (ee) of the unreacted starting material continually rises as more.