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1408168-77-3

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1408168-77-3 Usage

General Description

Potassium (2-acetoxyethyl)trifluoroborate is a chemical compound with the formula K[BF3CH2CH2OC(O)CH3]. It is a borate ester and contains potassium, boron, carbon, hydrogen, and oxygen atoms in its structure. PotassiuM (2-acetoxyethyl)trifluoroborate is commonly used in organic synthesis as a reagent for the preparation of organic compounds. It is also used in the production of pharmaceuticals, agrochemicals, and materials science. Potassium (2-acetoxyethyl)trifluoroborate is a versatile and valuable compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1408168-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,1,6 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1408168-77:
(9*1)+(8*4)+(7*0)+(6*8)+(5*1)+(4*6)+(3*8)+(2*7)+(1*7)=163
163 % 10 = 3
So 1408168-77-3 is a valid CAS Registry Number.

1408168-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Potassium (2-acetoxyethyl)(trifluoro)borate(1-)

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

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

More Details:1408168-77-3 SDS

1408168-77-3Upstream product

1408168-77-3Downstream Products

1408168-77-3Relevant articles and documents

Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: Access to aryl/heteroarylethyloxy motifs

Fleury-Bregeot, Nicolas,Presset, Marc,Beaumard, Floriane,Colombel, Virginie,Oehlrich, Daniel,Rombouts, Frederik,Molander, Gary A.

, p. 10399 - 10408 (2013/01/15)

The introduction of an alkoxyethyl moiety onto aromatic substructures has remained a long-standing challenge for synthetic organic chemists. The main reasons are the inherent instability of alkoxyethylmetallic species and the lack of general procedures to access them. A new method utilizing a cross-coupling strategy based on the exceptional properties of organotrifluoroborates has been developed, and the method allows an easy and efficient installation of this unit on a broad range of aryl and heteroaryl bromides.

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