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1-(naphthalen-2-yl)-3-(propylsulfonyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75910-39-3

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75910-39-3 Usage

Family

Chalcones

Pharmacological Activities

Anti-inflammatory
Anti-cancer
Anti-allergic

Inhibition of Inflammatory Cytokines

Yes

Potential Applications

Treatment of rheumatoid arthritis
Treatment of asthma
Treatment of cancer

Additional Effects

Antioxidant properties
Neuroprotective effects

Potential Applications in Neurodegenerative Diseases

Yes

Unique Chemical Structure

Yes

Interest in Medicinal Chemistry

High

Further Research and Development

Ongoing

Check Digit Verification of cas no

The CAS Registry Mumber 75910-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75910-39:
(7*7)+(6*5)+(5*9)+(4*1)+(3*0)+(2*3)+(1*9)=143
143 % 10 = 3
So 75910-39-3 is a valid CAS Registry Number.

75910-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-naphthalen-2-yl-3-propylsulfonylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1-(2-Naphthyl)-3-propansulfonyl-propen-(2)-on-(1)

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:75910-39-3 SDS

75910-39-3Relevant academic research and scientific papers

Reactions of &α,&β-Unsaturated &γ-Oxosulfones with Nucleophiles

Messinger, Paul,Greve, Harald

, p. 688 - 696 (2007/10/02)

Bromination of the γ-oxosulfones 1 and subsequent dehydrohalogenation leads to the α,β-unsaturated γ-oxosulfones 3.These products react with primary and secondary amines to yield the enaminoketones 7. γ-Oxobissulfones 10 are formed from 3 by addition of t

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