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(R)-BoroAbu-(+)-Pinanediol-HCl is a chiral chemical compound that features a pinanediol molecule with a boronic acid group attached to the alpha carbon. It exists as a hydrochloride salt and is recognized for its capacity to form boronate esters with diols, which is instrumental in various organic synthesis processes. (R)-BoroAbu-(+)-Pinanediol-HCl is particularly valuable in asymmetric catalysis, a technique critical for producing enantiomerically pure compounds, which are essential in pharmaceuticals and agrochemicals.

319009-92-2

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319009-92-2 Usage

Uses

Used in Pharmaceutical Synthesis:
(R)-BoroAbu-(+)-Pinanediol-HCl is used as a chiral reagent for the synthesis of pharmaceuticals, leveraging its ability to form boronate esters with diols. This property is crucial for creating enantiomerically pure compounds, which are necessary for the development of drugs with specific biological activities and reduced side effects.
Used in Agrochemical Synthesis:
In the agrochemical industry, (R)-BoroAbu-(+)-Pinanediol-HCl is utilized as a reagent in the synthesis of chiral pesticides and other agrochemicals. (R)-BoroAbu-(+)-Pinanediol-HCl's ability to participate in asymmetric catalysis ensures the production of enantiomerically pure active ingredients, which can target specific pests while minimizing harm to non-target organisms and the environment.
Used in Asymmetric Catalysis:
(R)-BoroAbu-(+)-Pinanediol-HCl is employed as a catalyst in asymmetric catalysis processes. Its chiral nature allows for the selective formation of one enantiomer over another, which is vital for creating compounds with specific biological activities and properties. This selective synthesis is particularly important in the production of high-value organic compounds with applications in various industries.
Used in Organic Synthesis:
Beyond its applications in pharmaceuticals and agrochemicals, (R)-BoroAbu-(+)-Pinanediol-HCl is used as a versatile reagent in organic synthesis for the creation of a wide range of high-value organic compounds. Its ability to form boronate esters with diols makes it a valuable tool for chemists in the synthesis of complex organic molecules with specific structural and functional requirements.

Check Digit Verification of cas no

The CAS Registry Mumber 319009-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,9,0,0 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 319009-92:
(8*3)+(7*1)+(6*9)+(5*0)+(4*0)+(3*9)+(2*9)+(1*2)=132
132 % 10 = 2
So 319009-92-2 is a valid CAS Registry Number.

319009-92-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-BoroAbu-(+)-Pinanediol-hydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:319009-92-2 SDS

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