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55436-41-4

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55436-41-4 Usage

Chemical class

Piperazine derivative It is a compound derived from the base structure of piperazine.

Structural features

Piperazine core with two benzo[1,3]dioxole groups attached The presence of these groups contributes to its potential biological activity.

Molecular weight

Approximately 360 g/mol Indicates the mass of one mole of the compound.

Appearance

Solid Describes the physical state of the compound at room temperature.

Solubility

Soluble in organic solvents It can dissolve in solvents like methanol, ethanol, or dimethyl sulfoxide (DMSO).

Potential applications

Medicinal chemistry and drug development Due to its structural features and the presence of biologically active moieties, it may have uses in the development of new pharmaceuticals.

Biological activity

Presence of piperazine and benzo[1,3]dioxole moieties These moieties are known to have biological activity, which may contribute to the compound's potential uses in medicine.

Further research

Pharmacological properties and potential uses Additional studies are needed to fully understand the compound's properties and how it can be applied in the medical field.

Safety and toxicity

Unknown The safety and toxicity profiles of 1,4-bis(benzo[1,3]dioxol-5-ylmethyl)piperazine have not been extensively studied and are not well-established. Caution should be exercised when handling and using this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 55436-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55436-41:
(7*5)+(6*5)+(5*4)+(4*3)+(3*6)+(2*4)+(1*1)=124
124 % 10 = 4
So 55436-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H22N2O4/c1-3-17-19(25-13-23-17)9-15(1)11-21-5-7-22(8-6-21)12-16-2-4-18-20(10-16)26-14-24-18/h1-4,9-10H,5-8,11-14H2

55436-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(1,3-benzodioxol-5-ylmethyl)piperazine

1.2 Other means of identification

Product number -
Other names 1,4-bis-piperonylpiperazine

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:55436-41-4 SDS

55436-41-4Relevant articles and documents

PLANT GROWTH-PROMOTION AGENT AND METHOD FOR PROMOTING PLANT GROWTH

-

Paragraph 0139; 0141; 0142; 0143, (2017/11/11)

The present invention concerns: a plant growth-promoting agent comprising a compound represented by Formula (I) or a salt thereof: wherein Ar1 represents a substituted or unsubstituted phenyl group, NZ represents a nitrogen-containing heterocyclic ring group or an acyclic nitrogen-containing group having a partial structure of the nitrogen-containing heterocyclic ring group, n is 0, 1, or 2, R1 and R2 each represent a hydrogen atom, a substituted or unsubstituted C1-3-alkyl group, a cyano group, or a carboxyl group, R1 and R2 may together form an oxo group, and when n is 2, R1 or R2 may be the same or different; and a method for promoting plant growth using the plant growth-promoting agent.

CONVENIENT SYNTHESIS OF N-BENZYL-N'-ACYL-PIPERAZINES

Gardini, G. P.,Palla, G.,Scapini, G.,Cesaroni, M. R.

, p. 887 - 890 (2007/10/02)

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Non anticholinergic gastric acid secretion inhibitors. New piperazine and related derivatives

Tricerri,Elitropi,Panto,et al.

, p. 555 - 562 (2007/10/08)

Some of the new piperazine derived compounds exhibited interesting gastric antisecretory properties without anticholinergic action. 1 Piperonyl 4 (3,7,11 trimethyl 2,6,10 dodecatrienyl) piperazine was the most active as an antisecretory agent in rat. Some analogous compounds, with the piperazine ring replaced by other heterocyclic or acyclic amines, were also prepared. Structure activity relationships are discussed.

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