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Boric acid triisopropyl ester, also known as triisopropyl borate, is a colorless liquid chemical compound with the molecular formula C9H21BO3. It is commonly used as a reagent in organic synthesis and as a catalyst in polymerization reactions. BORIC ACID TRIISOPROPYL ESTER is highly flammable and should be handled with care due to its low toxicity and potential to cause irritation to the skin, eyes, and respiratory system upon exposure. Additionally, it serves as a solvent and a precursor in the production of specialty chemicals and pharmaceuticals.

10298-87-0

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10298-87-0 Usage

Uses

Used in Organic Synthesis:
Boric acid triisopropyl ester is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of desired products in the synthesis process.
Used in Polymerization Reactions:
As a catalyst, boric acid triisopropyl ester is employed in polymerization reactions to accelerate the process and improve the efficiency of polymer formation, enhancing the properties of the resulting polymers.
Used in Solvent Applications:
Boric acid triisopropyl ester is utilized as a solvent in various chemical processes due to its ability to dissolve a wide range of substances, aiding in the smooth progression of reactions and extractions.
Used in Specialty Chemicals and Pharmaceuticals Production:
Boric acid triisopropyl ester serves as a precursor in the production of specialty chemicals and pharmaceuticals, playing a crucial role in the synthesis of these complex and high-value compounds.
Used in Research and Development:
In the field of research and development, boric acid triisopropyl ester is used to explore new chemical reactions, develop innovative synthetic pathways, and create novel materials with unique properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10298-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10298-87:
(7*1)+(6*0)+(5*2)+(4*9)+(3*8)+(2*8)+(1*7)=100
100 % 10 = 0
So 10298-87-0 is a valid CAS Registry Number.

10298-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tri-iso-propoxyboroxin

1.2 Other means of identification

Product number -
Other names 2,4,6-TRIISOPROPOXY-CYCLOTRIBOROXINE

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:10298-87-0 SDS

10298-87-0Relevant academic research and scientific papers

A new route to boron nitride

Economy,Anderson

, p. 989 - 992 (1966)

A new synthesis is described for preparation of boron nitride from the reaction of an alkyl polyborate-ammonia complex (RO)3B25O36·(NH3)8 with ammonia in the temperature range of 400-800°. The ammonia complex is obtained via a novel disproportionation of a trialkoxyboroxine to the corresponding trialkoxyborane and the ammonia complex. Boron nitride obtained under these conditions possesses a turbostratic structure.

PROCESS FOR SYNTHESIS OF DIALKOXYORGANOBORANES

-

Page/Page column 9, (2008/06/13)

The invention relates to a process for the synthesis of dialkoxyorganoboranes, in particular to a process for the synthesis of dialkoxyorganoboranes by an ester exchange reaction. Moreover, the invention relates to a process for the synthesis of organo-oxazaborolidine catalysts (organo-CBS) and of trialkylboroxins. Furthermore, the invention relates to methods of using dialkoxyorganoboranes for the preparation of organo-CBS catalysts and in Suzuki-type coupling reactions.

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