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Boronic acid, butyl-, dimethyl ester is an organic compound with the chemical formula C8H19BO2. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 157.05 g/mol. Boronic acid, butyl-, dimethyl ester is a derivative of boronic acid, featuring a butyl group and two methyl groups attached to the boron atom. It is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction. The compound is also known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as in materials science for the development of new polymers. Due to its reactivity and stability, it is a valuable building block in the creation of complex organic molecules.

2117-94-4

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2117-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2117-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2117-94:
(6*2)+(5*1)+(4*1)+(3*7)+(2*9)+(1*4)=64
64 % 10 = 4
So 2117-94-4 is a valid CAS Registry Number.

2117-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name butyldimethoxyborane

1.2 Other means of identification

Product number -
Other names butyl-dimethoxy-borane

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:2117-94-4 SDS

2117-94-4Relevant academic research and scientific papers

Polyfluoroorganoboron-oxygen compounds. 5 Feasible routes to perfluoroalkyltrimethoxyborates M[CnF2n+1B(OMe) 3] (n ≥ 3)

Adonin, Nicolay Yu.,Bardin, Vadim V.,Frohn, Hermann-Josef

, p. 647 - 652 (2007)

A well applicable preparative method for lithium perfluoroalkyltrimethoxyborates, Li[CnF2n+1B(OMe) 3] (n = 3, 4, 6), was elaborated which is based on the reaction of B(OMe)3 with CnF2n+1Li generated from C nF2n+1H and t-BuLi. Alternative perfluoroalkylation reactions of B(OMe)3 with perfluoropropyllithium generated from C3F7I and RLi, perfluoropropylmagnesium bromide, or perfluoropropyltrimethylsilane and potassium fluoride gave less satisfactory results for M[C3F7B(OMe)3]. The conversion of M[CnF2n+1B(OMe)3] salts (M = Li, BrMg) into K[CnF2n+1B(OMe)3] salts and basic properties of the new salts are reported.

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