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1-METHYL-4-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]PIPERAZINE, also known as 4-(4-Methyl-1-piperazinyl)benzeneboronic acid pinacol ester, is a chemical compound with a complex structure that features a piperazine ring and a boron-containing moiety. It is characterized by its potential reactivity and stability, which make it a valuable component in various chemical and pharmaceutical applications.

747413-21-4

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  • 1-Methyl-4-[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-YL)Phenyl]Piperazine

    Cas No: 747413-21-4

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747413-21-4 Usage

Uses

Used in Pharmaceutical Industry:
1-METHYL-4-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]PIPERAZINE is used as a pharmaceutical intermediate for the synthesis of various drugs and active pharmaceutical ingredients. Its unique structure allows it to serve as a building block in the development of new medications, particularly those targeting specific biological pathways or receptors.
As a pharmaceutical intermediate, 1-METHYL-4-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]PIPERAZINE plays a crucial role in the synthesis of drugs with potential therapeutic applications. Its versatility in chemical reactions enables the creation of a wide range of pharmaceutical compounds, contributing to the advancement of medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 747413-21-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,7,4,1 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 747413-21:
(8*7)+(7*4)+(6*7)+(5*4)+(4*1)+(3*3)+(2*2)+(1*1)=164
164 % 10 = 4
So 747413-21-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H27BN2O2/c1-16(2)17(3,4)22-18(21-16)14-6-8-15(9-7-14)20-12-10-19(5)11-13-20/h6-9H,10-13H2,1-5H3

747413-21-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H51659)  4-(4-Methyl-1-piperazinyl)benzeneboronic acid pinacol ester, 96%   

  • 747413-21-4

  • 1g

  • 771.0CNY

  • Detail
  • Alfa Aesar

  • (H51659)  4-(4-Methyl-1-piperazinyl)benzeneboronic acid pinacol ester, 96%   

  • 747413-21-4

  • 5g

  • 3057.0CNY

  • Detail

747413-21-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-4-[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-YL)Phenyl]Piperazine

1.2 Other means of identification

Product number -
Other names 1-METHYL-4-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]PIPERAZINE

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:747413-21-4 SDS

747413-21-4Downstream Products

747413-21-4Relevant articles and documents

Thiazolidine derivatives or salts thereof as an active ingredient an inhibitor Pim

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Paragraph 0651; 0652, (2018/10/19)

PROBLEM TO BE SOLVED: To provide compounds which have excellent Pim inhibitory action and are useful as pharmaceuticals.SOLUTION: A compound is a thiazolidine derivative represented by the general formula (1) in the figure, or a salt thereof. (In the formula, X represents O or S; Rrepresents a hydrogen atom or a Calkyl group; Z, Z, Z, Z, Zand Zeach independently represent CH or N; Y represents an optionally substituted, divalent Caromatic hydrocarbon group or the like; Am represents a disubstituted amino group, or an optionally substituted, nitrogen-containing saturated heterocyclic group; and Rand Reach independently represent a hydrogen atom, a halogen atom, an alkyl group or the like.)

Palladium-mediated conversion of para-aminoarylboronic esters into para-aminoaryl-11C-methanes

Andersen, Valdemar L.,Herth, Matthias M.,Lehel, Szabolcs,Knudsen, Gitte M.,Kristensen, Jesper L.

supporting information, p. 213 - 216 (2013/02/22)

Cross-couplings are an alternative to conventional 11C- methylations which are generally employed in PET tracer synthesis. Therefore, we set out to develop a general procedure for the synthesis of para- 11CH3 labeled aromatic amines from the corresponding para-aminoarylboronic esters in the presence of free amines. Aryl boronic esters containing primary, secondary, and tertiary amines were successfully converted into corresponding labeled methyl derivatives in sufficient radiochemical yield to apply this method for tracer development. This procedure was applied to the labeling of CIMBI-712, a promising candidate for the in vivo imaging of the 5-HT7 receptor in the CNS.

PEPTIDASE INHIBITORS

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, (2012/10/18)

Novel compounds of the formula (I) wherein R1, R2, D, A, B and X have the meanings defined herein, pharmaceutical compositions comprising them as active ingredient, as well as their use in medicine, in particular as peptidase inhibitors, more specifically

QUINOXALINE DERIVATIVES AS INHIBITORS OF THE TYROSINE KINASE ACTIVITY OF JANUS KINASES

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Page/Page column 49-50, (2009/01/24)

The present invention relates to quinoxaline compound of the formula (I): wherein R1 is carbocyclyl or heterocyclyl, either of which is optionally substituted with 1, 2, 3, 4 or 5 R7; R2 is carbocyclyl or heterocyclyl, either of which is optionally substituted with 1, 2, 3, 4 or 5 R8; R3, R4, R5 and R6 are each independently hydrogen or R9; and R7, R8 and R9 are each independently selected from organic and inorganic substituents, their use in therapy of diseases, in particular diseases mediated by the tyrosine kinase activity of Janus kinases, including JAK-2 and JAK-3 kinases

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