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1218790-99-8

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1218790-99-8 Usage

General Description

Piperidine-4-boronic acid pinacol ester HCl is a chemical compound that consists of a piperidine ring attached to a boronic acid group and a pinacol ester, all of which are bonded to a hydrogen chloride molecule. Piperidine-4-boronic acid pinacol ester HCl is commonly used in organic synthesis as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds. It is also used as a building block in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. The HCl salt form of this compound makes it more stable and easier to handle in the laboratory, allowing for greater control and precision in chemical reactions. Overall, piperidine-4-boronic acid pinacol ester HCl is a versatile and valuable chemical reagent with numerous applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1218790-99-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,8,7,9 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1218790-99:
(9*1)+(8*2)+(7*1)+(6*8)+(5*7)+(4*9)+(3*0)+(2*9)+(1*9)=178
178 % 10 = 8
So 1218790-99-8 is a valid CAS Registry Number.

1218790-99-8SDS

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 Piperidine-4-boronic acid pinacol ester HCl

1.2 Other means of identification

Product number -
Other names 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine hydrochloride

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:1218790-99-8 SDS

1218790-99-8Relevant articles and documents

Solvent-freeN-Boc deprotection byex situgeneration of hydrogen chloride gas

De Borggraeve, Wim M.,Gilles, Philippe,Van Mileghem, Seger,Verschueren, Rik H.

supporting information, p. 5782 - 5787 (2021/07/12)

An efficient, scalable and sustainable method for the quantitative deprotection of thetert-butyl carbamate (N-Boc) protecting group is described, using down to near-stoichiometric amounts of hydrogen chloride gas in solvent-free conditions. We demonstrate theex situgeneration of hydrogen chloride gas from sodium chloride and sulfuric acid in a two-chamber reactor, introducing a straightforward method for controlled and stoichiometric release of HCl gas. The solvent-free conditions allow deprotection of a wide variety ofN-Boc derivatives to obtain the hydrochloride salts in quantitative yields. The procedure obviates the need for any work-up or purification steps providing an uncomplicated green alternative to standard methods. Due to the solvent-free, anhydrous conditions, this method shows high tolerance towards acid sensitive functional groups and furnishes expanded functional group orthogonality.

INHIBITORS OF FATTY ACID AMIDE HYDROLASE

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Page/Page column 68, (2010/11/03)

Provided herein are compounds of formula (I): or pharmaceutically acceptable salts, solvates or prodrugs thereof or mixtures thereof, wherein Z1, Z2, X1, X2, X3, R1, R2 R3/

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