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1150655-04-1

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1150655-04-1 Usage

General Description

Potassium dimethylaminomethyltrifluoroborate is a specialized chemical compound, often used in the field of organic chemistry. This chemical, like other borate compounds, is a salt comprised of the potassium cation (K+) and the dimethylaminomethyltrifluoroborate anion. Its unique structure and properties make it useful for various organic synthesis processes, particularly those involving boron-based reactions. Some studies suggest it can serve as an efficient nucleophile for the construction of nitrogen-containing compounds. Despite its utility, it must be handled with care due to its potential reactivity and the need for appropriate safety measures in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 1150655-04-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,0,6,5 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1150655-04:
(9*1)+(8*1)+(7*5)+(6*0)+(5*6)+(4*5)+(3*5)+(2*0)+(1*4)=121
121 % 10 = 1
So 1150655-04-1 is a valid CAS Registry Number.

1150655-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium,(dimethylamino)methyl-trifluoroboranuide

1.2 Other means of identification

Product number -
Other names Potassium dimethylaminomethyltrifluoroboronate

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:1150655-04-1 SDS

1150655-04-1Upstream product

1150655-04-1Relevant articles and documents

A convergent strategy towards febrifugine and related compounds

Maiden,Mbelesi,Procopiou,Swanson,Harrity

, p. 4159 - 4169 (2018/06/12)

We report a modular five step synthetic route to the febrifugines that employs 2-(chloromethyl)allyl-trimethylsilane as a conjunctive reagent for the coupling of the piperidine and quinazolinone groups. We also demonstrate the application of a recent Rh-catalyzed quinazolinone synthesis for the facile generation of febrifugine analogs.

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