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1446-24-8

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1446-24-8 Usage

General Description

3-allylphenol is a chemical compound with the molecular formula C9H10O. It is a colorless to light yellow liquid with a strong, sweet, floral odor. 3-allylphenol is commonly used as a fragrance ingredient in perfumes, soaps, and other personal care products. It is also used in the production of flavorings, pharmaceuticals, and other chemicals. However, it is important to note that 3-allylphenol is a potentially hazardous chemical and should be handled with care. Exposure to high concentrations of this chemical can cause irritation to the skin, eyes, and respiratory tract. Additionally, 3-allylphenol is considered to be a possible human carcinogen based on studies conducted on animals. Therefore, proper safety precautions should be taken when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 1446-24-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1446-24:
(6*1)+(5*4)+(4*4)+(3*6)+(2*2)+(1*4)=68
68 % 10 = 8
So 1446-24-8 is a valid CAS Registry Number.

1446-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-prop-2-enylphenol

1.2 Other means of identification

Product number -
Other names m-Allylphenol

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:1446-24-8 SDS

1446-24-8Relevant articles and documents

Structure–activity relationships and docking studies of hydroxychavicol and its analogs as xanthine oxidase inhibitors

Nishiwaki, Keiji,Ohigashi, Kanae,Deguchi, Takahiro,Murata, Kazuya,Nakamura, Shinya,Matsuda, Hideaki,Nakanishi, Isao

, p. 741 - 747 (2018/07/05)

Hydroxychavicol (HC), which is obtained from the leaves of Piper betle LINN. (Piperaceae), inhibits xanthine oxidase (XO) with an IC50 value of 16.7μM, making it more potent than the clinically used allopurinol (IC50=30.7μM). Herein, a structure–activity relationship analysis of the polar part analogs of HC was conducted and an inhibitor was discovered with a potency 13 times that of HC. Kinetic studies have revealed that HC and its active analog inhibit XO in an uncompetitive manner. The binding structure prediction of these inhibitor molecules to the XO complex with xanthine suggested that both compounds (HC and its analog) could simultaneously form hydrogen bonds with xanthine and XO.

ASPARTYL PROTEASE INHIBITORS

-

, (2009/01/20)

The invention provides compounds of the formula (I) N-oxides, addition salts, quaternary amines, metal complexes, stereochemically isomeric forms and metabolites thereof, wherein G is-O-, -S(=O)r-, -CRdRd or -NRa-; W is H, C1-C6

The synthesis of phenolic propane-1, 2- and 1,3-diols as intermediates in immobilised chelatants for the borate anion

Tyman, John H. P.,Payne

, p. 691 - 695 (2007/10/03)

The isomeric 3-(hydroxyphenyl)propane-1, 2-diols have been synthesised from allylic precursors by epoxidation and cleavage. Several different methods have been examined for obtaining 1-(methoxyphenyl)propane-1, 3-diols. 2-(methoxyphenyl)propane-1, 3-diols and certain hydroxy analogues have been obtained from benzaldoximes converted by oxidation to methoxy- and benzyloxynitromethylbenzenes followed by hydroxymethylation with formaldehyde and catalytic hydrogenation.

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