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Benzenemethanol, α-ethenyl-3-phenoxy-, also known as 3-phenoxy-α-vinylbenzyl alcohol or 3-phenoxy-α-vinylbenzenemethanol, is an organic compound with the chemical formula C15H14O2. It is a colorless to pale yellow liquid with a molecular weight of 226.27 g/mol. Benzenemethanol, a-ethenyl-3-phenoxy- is characterized by the presence of a benzyl alcohol group (C6H5CH2OH) and a phenoxy group (C6H5O) attached to a vinyl group (C2H3). It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive functional groups, it can undergo a variety of chemical reactions, such as esterification, etherification, and condensation, making it a versatile building block in organic synthesis.

60148-63-2

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60148-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60148-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60148-63:
(7*6)+(6*0)+(5*1)+(4*4)+(3*8)+(2*6)+(1*3)=102
102 % 10 = 2
So 60148-63-2 is a valid CAS Registry Number.

60148-63-2SDS

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 1-(3-phenoxyphenyl)prop-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 1-(3-phenoxyphenyl)-2-propen-1-ol

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:60148-63-2 SDS

60148-63-2Relevant articles and documents

PYRETHROID COMPOUND, AND HAIR RESTORER AND HAIR RESTORER COMPOSITION COMPRISING THE SAME

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Paragraph 0028; 0029, (2017/08/26)

PROBLEM TO BE SOLVED: To provide a pyrethroid compound having hair growth effect. SOLUTION: The present invention provides a pyrethroid compound represented by general formula (1) [in general formula (1), R1 is selected from a hydrogen atom, a halogen atom, an azido group, an alkoxy group having 1 to 4 carbon atoms, and an alkyl group having 1 to 4 carbon atoms, R2 is selected from a methyl group, an ethyl group and an isopropyl group, R3 is selected from -C≡N, -C≡CH, -C≡C-CH3 and -CH=CH2, and R4 is selected from a methyl group, a phenyl group, a 2-methoxy ethyl group, a methoxymethyl group, and a propargyl group]. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

A facile synthesis of α-fluoro ketones catalyzed by [Cp*IrCl2]2

Ahlsten, Nanna,Bartoszewicz, Agnieszka,Agrawal, Santosh,Martin-Matute, Belen

supporting information; experimental part, p. 2600 - 2608 (2011/10/02)

Allylic alcohols are isomerized into enolates (enols) by [Cp*IrCl2]2. The enolates react with Selectfluor present in the reaction media. This method produces α-fluoro ketones as single constitutional isomers in high yields. Georg Thieme Verlag Stuttgart. New York.

Building molecular complexity via tandem ru-catalyzed isomerization/C-H activation

Bartoszewicz, Agnieszka,Martin-Matute, Belen

supporting information; experimental part, p. 1749 - 1752 (2009/09/06)

A tandem isomerization/C-H activation of a My lie alcohols was performed using a catalytic amount of RuCI2(PPh3)3. A variety of ortho alkylated ketones have been obtained in excellent yields. This tandem process relies on an in situ generation of a carbonyl functional group that directs the ortho C-H bond activation.

Process for the preparation of insecticidally active diphenylether compounds

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, (2008/06/13)

This invention relates to a process for the preparation of insecticidally active compounds and to novel styrene derivatives useful as intermediates therein.

Insecticidal benzylfurylmethyl esters of 3-(2,2-dichlorovinyl)-2,2-dimethyl-cyclopropane carboxylic acids

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, (2008/06/13)

Novel carboxylic acid esters of the formula STR1 where R1, R2 and R3 are identical or different and each is hydrogen, halogen or alkyl or alkenyl of up to 5 carbon atoms, Y is 3-(2,2-dihalogenovinyl)-2,2-dimethyl-cycloprop

Vinylcyclopropanecarboxylic acid-3-phenoxy-α-vinylbenzyl esters, processes for producing them, and their use in combating pests

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, (2008/06/13)

Vinylcyclopropanecarboxylic acid-3-phenoxy-α-vinylbenzyl esters of the formula STR1 in which X1 is fluorine, chlorine or bromine, X2 is hydrogen or bromine, and Y is hydrogen or methyl, processes for producing them, and their use in

Cyclopropanecarboxylic acid-phenoxy-α-vinyl-benzyl esters, processes for producing them, and their use in combating pests

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, (2008/06/13)

Cyclopropanecarboxylic acid-phenoxy-α-vinyl-benzyl esters of the formula STR1 in which Y is chlorine or bromine, and R1 is --CH=CH2 or STR2 processes for producing them, and their use in combating pests.

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