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2-Hydroxy-3-(2-methyl-2-propenyl)benzaldehyde is a distinctive organic compound with the molecular formula C11H12O2. It is a member of the benzaldehydes class, characterized by an aromatic benzene ring with a formyl (aldehyde) group attached to one of the carbon atoms. 2-Hydroxy-3-(2-methyl-2-propenyl)benzaldehyde is distinguished by the presence of a hydroxy group and a 2-methyl-2-propenyl group on the benzene ring. Its aldehyde group endows it with carbonyl properties, while the hydroxy group suggests it may also exhibit alcoholic characteristics. The specific chemical behavior, applications, and properties of 2-Hydroxy-3-(2-methyl-2-propenyl)benzaldehyde can vary depending on environmental conditions and interactions with other compounds.

162971-77-9

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162971-77-9 Usage

Uses

Used in Chemical Research and Synthesis:
2-Hydroxy-3-(2-methyl-2-propenyl)benzaldehyde is utilized as a key intermediate in the synthesis of various organic compounds for research purposes. Its unique structure allows for versatile chemical reactions, making it valuable in the development of new chemical entities and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Hydroxy-3-(2-methyl-2-propenyl)benzaldehyde is employed as a building block for the creation of novel drug molecules. Its functional groups can be manipulated to form complex organic compounds with potential medicinal properties.
Used in Flavor and Fragrance Industry:
Due to its aromatic nature, 2-Hydroxy-3-(2-methyl-2-propenyl)benzaldehyde is used as a component in the formulation of fragrances and flavors. Its distinct chemical structure contributes to the creation of unique scents and tastes in various consumer products.
Used in Material Science:
In material science, 2-Hydroxy-3-(2-methyl-2-propenyl)benzaldehyde may be incorporated into the development of advanced materials with specific properties, such as polymers with tailored characteristics for use in coatings, adhesives, or composites.

Check Digit Verification of cas no

The CAS Registry Mumber 162971-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,7 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 162971-77:
(8*1)+(7*6)+(6*2)+(5*9)+(4*7)+(3*1)+(2*7)+(1*7)=159
159 % 10 = 9
So 162971-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O2/c1-8(2)6-9-4-3-5-10(7-12)11(9)13/h3-5,7,13H,1,6H2,2H3

162971-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-3-(2-methylprop-2-enyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2-hydroxy-3-(2-methyl-2-propenyl)

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:162971-77-9 SDS

162971-77-9Relevant academic research and scientific papers

Synthesis and cytotoxic activity of novel 2,6-disubstituted-4-mor- pholinothieno[3,2-d]pyrimidines as potent anti-tumor agents

Zhu, Wu Fu,Zhai, Xin,Li, Sai,Cao, Yun Yun,Gong, Ping,Liu, Ya Jing

, p. 703 - 706 (2012/07/16)

A series of 2,6-disubstituted-4-morpholinothieno[3,2-d]pyrimidine derivatives were synthesized and their cytotoxic activity against H460, HT-29, MDA-MB-231, U87MG and H1975 cancer cell lines were evaluated in vitro. Most of the target compounds exhibited moderate to excellent activity to the tested cell lines. The most promising compound 23 (0.84 μmol/L, 0.23 μmol/L, 2.52 μmol/L, 1.80 μmol/L) was 1.0, 2.9, 29.3 and 4.3 times more active than GDC-0941 (0.87 μmol/L, 0.66 μmol/L, 73.8 μmol/L, 7.77 μmol/L) against H460, HT-29, MDA-MB-231 and U87MG cell lines, respectively.

Facile aromatic Claisen rearrangement catalysed by tin(IV) chloride

Sarkar, Debayan,Venkateswaran, Ramanathapuram V.

, p. 653 - 654 (2008/12/20)

Allyl aryl ethers undergo facile Claisen rearrangement under mild conditions catalysed by tin(IV) chloride. Georg Thieme Verlag Stuttgart.

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