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3179-08-6

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3179-08-6 Usage

General Description

4-HYDROXY-B-NITROSTYRENE is a chemical compound with the molecular formula C8H7NO4. It is a nitroalkene derivative, which means it contains a nitro group attached to an alkene group. It is commonly used in organic synthesis and medicinal chemistry research due to its potential applications as a building block in the synthesis of various organic molecules. 4-HYDROXY-B-NITROSTYRENE is known for its strong electron-withdrawing and -donating properties, as well as its potential as a Michael acceptor in organic reactions. It may also have potential biological activity and is therefore of interest to researchers in the pharmaceutical industry. However, it is important to handle this compound with caution due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 3179-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3179-08:
(6*3)+(5*1)+(4*7)+(3*9)+(2*0)+(1*8)=86
86 % 10 = 6
So 3179-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO3/c10-8-3-1-7(2-4-8)5-6-9(11)12/h1-6,10H/b6-5+

3179-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-β-nitrostyrene

1.2 Other means of identification

Product number -
Other names 4-HYDROXY-B-NITROSTYRENE

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:3179-08-6 SDS

3179-08-6Relevant articles and documents

Efficient bifunctional nanocatalysts by simple postgrafting of spatially isolated catalytic groups on mesoporous materials

Sharma, Krishna K.,Asefa, Tewodros

, p. 2879 - 2882 (2007)

(Chemical Equation Presented) Hard graft pays off for Henry: An efficient acid-base bifunctional mesoporous catalyst was prepared by one-step post-synthesis grafting of aminoorganoalkoxysilane groups on mesoporous silica (see picture). The catalyst led to

Access to C5-Alkylated Indolines/Indoles via Michael-Type Friedel-Crafts Alkylation Using Aryl-Nitroolefins

Ertugrul, Berrak,Kilic, Haydar,Lafzi, Farrokh,Saracoglu, Nurullah

, p. 9018 - 9038 (2018/06/27)

A straightforward synthetic route toward C5-alkylated indolines/indoles has been developed. The strategy is composed of Zn(OTf)2-catalyzed Friedel-Crafts alkylation of N-benzylindolines with nitroolefins, and a series of diverse indolines was first obtained in up to 99% yield. This reaction provides a direct and practical route to a variety of the C5-alkylated indolines which were also utilized for accessing corresponding indoles. Indoline derivatives with free NH groups could be obtained through an N-deprotection reaction. Moreover, the primary alkyl nitro groups in both indolines and indoles are amenable to further synthetic elaborations, thereby broadening the diversity of the products.

METHODS AND COMPOSITIONS FOR SELECTIVE AND TARGETED CANCER THERAPY

-

Page/Page column 227, (2015/03/28)

Provided herein are methods and compositions for selective and targeted cancer therapy, in particular certain benzothiophenes, benzothiazoles, oxalamides, N-acyl ureas and chromones, and their use in selectively treating certain adenocarcinomas. In some embodiments, the selective toxicity of the compounds may be mediated through SCD1 and/or CYP450 such as CYP4F11.

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