More research is needed about [1,4′-Bipiperidine]-1′-carbonyl chloride

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Computed Properties of C11H19ClN2O

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Computed Properties of C11H19ClN2O, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 103816-19-9, Name is [1,4′-Bipiperidine]-1′-carbonyl chloride, molecular formula is C11H19ClN2O. In a Patent, authors is ，once mentioned of 103816-19-9

New camptothecin derivatives possessing high anti-tumor activity with slight toxicity, represented by the general formula: STR1 wherein R1 is a hydrogen atom, a halogen atom or an alkyl group with 1-4 carbon atoms and X is a chlorine atom or –NR2 R3 where R2 and R3 are the same or different and each represents a hydrogen atom, a substituted or unsubstituted alkyl group with 1-4 carbon atoms or a substituted or unsubstituted carbocyclic or heterocyclic group, with the proviso that when both R2 and R3 are the substituted or unsubstituted alkyl groups, they may be combined together with the nitrogen atom, to which they are bonded, to form a heterocyclic ring which may be interrupted with –O–, –S– and/or >N–R4 in which R4 is a hydrogen atom, a substituted or unsubstituted alkyl group with 1-4 carbon atoms or a substituted or unsubstituted phenyl group and wherein the grouping –O–CO–X is bonded to a carbon atom located in any of the 9-, 10- and 11-positions in the ring A of camptothecin, as well as an ammonium salt or an alkali metal salt thereof. These new camptothecin derivatives are prepared by reacting a 7-R1 -camptothecin derivative having a hydroxyl group in any of the 9-, 10- and 11-positions on the ring A thereof with phosgen and then reacting, if necessary, the resultant 7-R1 -camptothecin derivative having a chlorocarbonyloxy group in the same position on the ring A thereof with an amine HNR2 R3 or by reacting a 7-R1 -camptothecin derivative having a hydroxyl group in any of the 9-, 10- and 11-positions on the ring A thereof with a carbamoyl chloride Cl-CONR2 R3.

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Computed Properties of C11H19ClN2O

Reference：
Piperidine – Wikipedia,
Piperidine | C5H18710N – PubChem