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3,5-diallyl-2-hydroxy-benzaldehyde, also known as Diallylhydroxybenzaldehyde (DAB), is a chemical compound with the molecular formula C15H16O2. It is a yellow liquid with a distinct odor and is commonly used in the production of perfumes and flavorings. DAB has been studied for its potential applications in pharmaceuticals and is known for its antimicrobial, antioxidant, and anti-inflammatory properties. It has also shown promise as a potential anti-cancer agent. Additionally, DAB has been investigated for its potential as a food preservative due to its ability to inhibit the growth of harmful bacteria and fungi. Overall, 3,5-diallyl-2-hydroxy-benzaldehyde is a versatile compound with a range of potential uses in various industries.

159968-52-2

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159968-52-2 Usage

Uses

Used in Perfume and Flavoring Industry:
3,5-diallyl-2-hydroxy-benzaldehyde is used as a key ingredient for creating distinct scents and flavors in perfumes and flavorings due to its unique odor and yellow color.
Used in Pharmaceutical Industry:
3,5-diallyl-2-hydroxy-benzaldehyde is used as a potential therapeutic agent for its antimicrobial, antioxidant, and anti-inflammatory properties. It is also being studied for its potential as an anti-cancer agent.
Used in Food Preservation:
3,5-diallyl-2-hydroxy-benzaldehyde is used as a natural food preservative to inhibit the growth of harmful bacteria and fungi, thereby extending the shelf life of food products.

Check Digit Verification of cas no

The CAS Registry Mumber 159968-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,9,6 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 159968-52:
(8*1)+(7*5)+(6*9)+(5*9)+(4*6)+(3*8)+(2*5)+(1*2)=202
202 % 10 = 2
So 159968-52-2 is a valid CAS Registry Number.

159968-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,4-diazepan-1-ylmethyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 3,5-diallylsalicylaldehyde

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:159968-52-2 SDS

159968-52-2Relevant academic research and scientific papers

Procaspase-3 activation as an anti-cancer strategy: Structure-activity relationship of procaspase-activating compound 1 (PAC-1) and its cellular co-localization with caspase-3

Peterson, Quinn P.,Hsu, Danny C.,Goode, David R.,Novotny, Chris J.,Totten, Ryan K.,Hergenrother, Paul J.

supporting information; experimental part, p. 5721 - 5731 (2010/02/28)

A goal of personalized medicine as applied to oncology is to identify compounds that exploit a defined molecular defect in a cancerous cell. A compound called procaspase-activating compound 1 (PAC-1) was reported that enhances the activity of procaspase-3 in vitro and induces apoptotic death in cancer cells in culture and inmouse xenograft models. Experimental evidence indicates that PAC-1 activates procaspase-3 in vitro through chelation of inhibitory zinc ions. Described herein is the synthesis and biological activity of a family of PAC-1 derivativeswhere key functional groups have been systematically altered. Analysis of these compounds reveals a strong correlation between the in vitro procaspase-3 activating effect and their ability to induce death in cancer cells in culture. Importantly, we also show that a fluorescently labeled version of PAC-1 co-localizes with sites of caspase-3 activity in cancer cells. The data presented herein further bolster the hypothesis that PAC-1 induces apoptosis in cancer cells through the direct activation of procaspase-3, has implications for the design and discovery of next-generation procaspase-3 activating compounds, and sheds light on the anti-apoptotic role of cellular zinc.

COMPOSITIONS AND METHODS INCLUDING CELL DEATH INDUCERS AND PROCASPASE ACTIVATION

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Page/Page column 70, (2008/12/08)

Compositions and methods are disclosed in embodiments relating to induction of cell death such as in cancer cells. Compounds and related methods for synthesis and use thereof, including the use of compounds in therapy for the treatment of cancer and selective induction of apoptosis in cells are disclosed. Compounds are disclosed in connection with modification of procaspases such as procaspase-3. In embodiments, compositions are capable of activation of procaspase-3.

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