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2-(4-BOC-PIPERAZINO-1-YL)-5-FLUOROBENZALDEHYDE is a chemical compound that is commonly used in medicinal chemistry and pharmaceutical research. It consists of a 5-fluorobenzaldehyde group attached to a piperazine ring with a tert-butoxycarbonyl (BOC) protecting group. The piperazine ring makes it a potential candidate for drug development due to its ability to interact with biological targets. The 5-fluorobenzaldehyde group also provides a useful synthetic handle for further modifications and can be used as a precursor for various pharmaceutical compounds. Overall, 2-(4-BOC-PIPERAZINO-1-YL)-5-FLUOROBENZALDEHYDE is a valuable intermediate in the synthesis of potential drug candidates and has applications in medicinal and synthetic chemistry.

697305-53-6

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697305-53-6 Usage

Uses

Used in Medicinal Chemistry:
2-(4-BOC-PIPERAZINO-1-YL)-5-FLUOROBENZALDEHYDE is used as a valuable intermediate for the synthesis of potential drug candidates due to its ability to interact with biological targets.
Used in Pharmaceutical Research:
2-(4-BOC-PIPERAZINO-1-YL)-5-FLUOROBENZALDEHYDE is used as a precursor for various pharmaceutical compounds, providing a useful synthetic handle for further modifications.

Check Digit Verification of cas no

The CAS Registry Mumber 697305-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,7,3,0 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 697305-53:
(8*6)+(7*9)+(6*7)+(5*3)+(4*0)+(3*5)+(2*5)+(1*3)=196
196 % 10 = 6
So 697305-53-6 is a valid CAS Registry Number.

697305-53-6SDS

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 tert-butyl 4-(4-fluoro-2-formylphenyl)piperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 2-(4-Boc-piperazine-1-yl)-5-fluorobenzaldehyde

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:697305-53-6 SDS

697305-53-6Relevant academic research and scientific papers

3-(5-METHOXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF

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, (2021/06/26)

The present disclosure relates to compounds of formula (I') and pharmaceutical compositions and their use in reducing Widely Interspaced Zinc Finger Motifs (WIZ) expression levels, or inducing fetal hemoglobin (HbF) expression, and in the treatment of inherited blood disorders (e.g., hemoglobinopathies, e.g., beta-hemoglobinopathies), such as sickle cell disease and beta-thalassemia.

Arylpropionylpiperazines as antagonists of the human melanocortin-4 receptor

Jiang, Wanlong,Tucci, Fabio C.,Chen, Caroline W.,Arellano, Melissa,Tran, Joe A.,White, Nicole S.,Marinkovic, Dragan,Pontillo, Joseph,Fleck, Beth A.,Wen, Jenny,Saunders, John,Madan, Ajay,Foster, Alan C.,Chen, Chen

, p. 4674 - 4678 (2007/10/03)

A series of 3-arylpropionylpiperazines were synthesized as antagonists of the melanocortin-4 receptor. Their potency was found to be increased by replacing the α-methyl substituent of the initial lead 11 with a larger s-Bu or i-Bu group. Further potency enhancement was observed when a glycine or β-alanine was incorporated onto the benzylamine. Some compounds demonstrated good potency, moderate selectivity, and oral bioavailability.

Practical asymmetric synthesis of α-branched 2- piperazinylbenzylamines by 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines

Jiang, Wanlong,Chen, Chen,Marinkovic, Dragan,Tran, Joe A.,Chen, Caroline W.,Arellano, L. Melissa,White, Nicole S.,Tucci, Fabio C.

, p. 8924 - 8931 (2007/10/03)

2-[4-(tert-Butoxycarbonyl)piperazinyl] benzylidene-tert-butanesulfinamides underwent nucleophilic 1,2-addition with different organometallic reagents to give highly diastereomerically enriched adducts. X-ray crystallography of the resulting α-branched N-B

AMINE COMPOUNDS

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Page 165-166, (2010/02/07)

The present invention provide a compound of the formula:wherein ring A represents an aromatic ring optionally having substituents; B, Y and Ya are the same or different and each represents a bond, etc.; R1 and R2 are the same or different and each represents a hydrogen atom, etc.; R3 represents a hydrogen atom, etc.; R4 and R5 are the same or different and each represents a hydrogen, etc.; R6 represents an indolyl group optionally having substituents; and Z and Za are the same or different and each represents a hydrogen atom, etc.; or a salt thereof or a prodrug thereof, having a somatostatin receptor binding inhibition activity and is useful for preventing and/or treating diseases associated with somatostatin.

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