Allylboronic acid pinacol ester CAS:72824-04-5-custom synthesis contract manufacturing
Allylboronic acid pinacol ester CAS:72824-04-5
Structural Formula Allylboronic acid pinacol ester CAS:72824-04-5
Product Name Allylboronic acid pinacol ester
Synonym Allylboronic acid pinacol ester;4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane;Allylboronic acid pinacol ester;Allylboronic acid pinacol ester
CAS No. 72824-04-5
Molecular Weight See details
Specifications Upon request
Packing Sea or Airworthy packing
Material Safety Data Sheet Upon request
Availability Please send your inquiry to info@nbinno.com

Product Name: Allylboronic acid pinacol ester
Other Name:
Allylboronic acid pinacol ester
4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane
CAS No: 72824-04-5
MF: C9H17BO2
MW: 168.04100
Density: 0.896 g/mL at 25 °C(lit.)
Boiling point: 50-53 °C5 mm Hg(lit.)
Flash point: 115 °F
Refractive index: n20/D 1.4268(lit.)
UN Number: Non-dangerous goods
Transport hazard class: Non-dangerous goods
Packing group: Non-dangerous goods
 
Specification
Appearance: Colorless transparent liquid
Assay: ≥98.0%
Water: ≤0.50%
 
Application
Be used as pharmaceutical intermediate.
A cobalt-catalyzed regioselective hydroxyethylation reaction of a diene with an olefin, a photocatalytic reaction using a nucleic acid as a template for energy transfer, and an indium-catalyzed stereoselective Hosomi-Sakurai reaction.
It is used to prepare cyclized sulfone hydroxyethylamine as a BACE1 inhibitor for the reduction reaction of amyloid β-peptide.
The metallization conversion reaction of carbene Ru iodide with silver carboxylate provides an activated C-H-Ru carbene complex as a catalyst for the Z-selective olefin metathesis reaction.
 
Package: 25kg/drum, can also be designed according to customer requirements.
Storage: Store in cool place. Keep container tightly closed in a dry and well-ventilated place.

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It involves demanding processes including high pressure hydrogenation, oxygen free water environment, ultra low temperature environment and highly corrosive environmentWe are the premier choice for all your chemical needs, we offer products with the tightest specifications in the industry to make your work easier.By following our guiding principles of Samples, Quotes, Literature, and Innovation, we are able to make continual process improvements for customers.The company's products have been exported to Europe, America, Southeast Asia, the Middle East, South America and other places, and established a long-term cooperative relationship with customers.The company is mainly engaged in pharmaceutical R&D outsourcing services, and continues to research and develop new products and technologies, providing project technology and sample preparation services for large and well-known pharmaceutical companies at home and abroad.


Experienced Reaction
AlkylationPolymerizationDiazotization
NeutrallzationSulfonationDecompose
NitrationEliminationEsterification
AdditionChlorinationSubstitution
DehydrogenationReductionHydrogenation
Oxidation
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