87249-60-3 Usage
Description
(S)-(+)-PINANEDIOL (DICHLORMETHYL)BORONATE is a chiral boron reagent utilized in organic synthesis and catalysis. It is composed of pinanediol, a bicyclic compound with a chiral center, and dichloromethylboronate. This reagent is widely recognized for its role in the asymmetric synthesis of various compounds, such as pharmaceuticals and agrochemicals. The boron component facilitates selective activation of specific functional groups through boron-mediated transformations, allowing for the creation of complex molecules with high enantioselectivity. Its distinctive structure and reactivity render it an indispensable tool in organic chemistry for the preparation of chiral compounds.
Uses
Used in Pharmaceutical Industry:
(S)-(+)-PINANEDIOL (DICHLORMETHYL)BORONATE is used as a key reagent for the asymmetric synthesis of pharmaceutical compounds. Its ability to selectively activate functional groups and promote the formation of complex molecules with high enantioselectivity makes it a valuable asset in the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-(+)-PINANEDIOL (DICHLORMETHYL)BORONATE is employed as a catalyst in the synthesis of various agrochemicals. Its chiral nature and capacity for selective activation of functional groups contribute to the development of more effective and targeted agrochemicals, enhancing crop protection and yield.
Used in Organic Synthesis:
(S)-(+)-PINANEDIOL (DICHLORMETHYL)BORONATE is utilized as a versatile reagent in organic synthesis, particularly for the preparation of chiral compounds. Its unique structure and reactivity enable the formation of complex molecules with high enantioselectivity, which is crucial for the development of enantiomerically pure compounds with specific biological activities.
Used in Catalysis:
As a chiral boron reagent, (S)-(+)-PINANEDIOL (DICHLORMETHYL)BORONATE is also used in catalysis to promote selective transformations and enhance the efficiency of various chemical reactions. Its ability to activate specific functional groups and control enantioselectivity makes it a valuable catalyst in the synthesis of enantiomerically pure compounds for various applications, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 87249-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,4 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87249-60:
(7*8)+(6*7)+(5*2)+(4*4)+(3*9)+(2*6)+(1*0)=163
163 % 10 = 3
So 87249-60-3 is a valid CAS Registry Number.
