(1R,2R,3S,5R)-Pinanediol Pyrrolidine-2S-boronate Hydrochloride

Product Name (1R,2R,3S,5R)-Pinanediol Pyrrolidine-2S-boronate Hydrochloride
CAT No. CS-T-60592
CAS No. 149716-73-4
Category Impurities
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles B1(OC2CC3CC(C3(C)C)C2(O1)C)C4CCCN4.Cl
InchIKey OVVMNBVQOPZMPY-NTEAFONJSA-N
Inchl InChI=1S/C14H24BNO2.ClH/c1-13(2)9-7-10(13)14(3)11(8-9)17-15(18-14)12-5-4-6-16-12;/h9-12,16H,4-8H2,1-3H3;1H/t9-,10-,11+,12-,14-;/m1./s1
IUPAC (2S)-2-[(1R,2R,6S,8R)-2,9,9-trimethyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decan-4-yl]pyrrolidine;hydrochloride
Controlled No
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(1R,2R,3S,5R)-Pinanediol Pyrrolidine-2S-boronate Hydrochloride is a chemical compound commonly used in organic synthesis. It is a boronic acid derivative with a pyrrolidine ring and a pinanediol moiety, which makes it a chiral compound. The hydrochloride salt is the most commonly used form of the compound due to its higher solubility in water. This compound is widely used in the field of pharmaceuticals as a chiral building block in the synthesis of various biologically active molecules. It is also used in the preparation of chiral ligands, which are important in asymmetric catalysis. The pinanediol moiety provides a chiral center, which allows for the production of enantiomerically pure compounds. The boronic acid group in (1R,2R,3S,5R)-Pinanediol Pyrrolidine-2S-b

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