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Benzenemethanol, 4-[(phenylmethyl)thio]-, also known as 4-(benzylthio)benzyl alcohol or 4-(phenylmethylthio)benzenemethanol, is an organic compound with the chemical formula C14H14OS. It is a colorless to pale yellow liquid with a molecular weight of 226.33 g/mol. Benzenemethanol, 4-[(phenylmethyl)thio]- is characterized by the presence of a benzyl alcohol group (C6H5CH2OH) and a benzylthio group (C6H5CH2S) attached to a benzene ring. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and functional groups, it can undergo various chemical reactions, such as oxidation, reduction, and substitution, making it a versatile building block in organic synthesis.

3448-98-4

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3448-98-4 Usage

Chemical compound

Benzenemethanol, 4-[(phenylmethyl)thio]-

Check Digit Verification of cas no

The CAS Registry Mumber 3448-98-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3448-98:
(6*3)+(5*4)+(4*4)+(3*8)+(2*9)+(1*8)=104
104 % 10 = 4
So 3448-98-4 is a valid CAS Registry Number.

3448-98-4SDS

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 (4-(benzylthio)phenyl)methanol

1.2 Other means of identification

Product number -
Other names 4-(benzylthio)phenyl methanol

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:3448-98-4 SDS

3448-98-4Relevant academic research and scientific papers

Metal acetylacetonates covalently anchored onto amine functionalized silica/starch composite for the one-pot thioetherification and synthesis of 2H-indazoles

Sodhi, Ravinderpal Kour,Changotra, Avtar,Paul, Satya

, p. 1819 - 1831 (2015/02/19)

This paper reports a series of novel metal acetylacetonates covalently anchored onto amine functionalized silica/starch composite, prepared by the Schiff condensation of metal acetylacetonates [Co(acac)2, Cu(acac)2, Pd(acac)2, Ru(acac)3, Mn(acac)3, Co(acac)3] with organically modified 3-aminopropyl silica/starch composite. Different metal acetylacetonates have been chosen with a view to select the most active heterogeneous catalyst. Among various catalysts, covalently anchored Cu(acac)2 onto amine functionalized silica/starch composite [ASS-Cu(acac)2] was found to be the most active and recyclable catalyst for the one-pot thioetherification and one-pot three component synthesis of 2H-indazoles via consecutive C-N and N-N bond formations. All the catalysts were characterized by FTIR, TGA and AAS analysis and the most active catalyst, [ASS-Cu(acac)2] was further characterized by SEM and TEM. The catalyst could be recovered by simple filtration and reused with almost consistent activity for four consecutive runs.

NAPHTHYLACETIC ACIDS

-

Page/Page column 89-90, (2010/06/15)

The invention is concerned with the compounds of formula (I) and pharmaceutically acceptable salts and esters thereof, wherein X, Q, and R1-R6 are defined in the detailed description and claims. In addition, the present invention relates to methods of manufacturing and using the compounds of formula (I) as well as pharmaceutical compositions containing such compounds. The compounds of formula (I) are antagonists or partial agonists at the CRTH2 receptor and may be useful in treating diseases and disorders associated with that receptor such as asthma.

A simple one-pot synthesis of hydroxylated and carboxylated aryl alkyl sulfides from various bromobenzenes

Ko, Jaeyoung,Ham, Jungyeob,Yang, Inho,Chin, Jungwook,Nam, Sang-Jip,Kang, Heonjoong

, p. 7101 - 7106 (2007/10/03)

A simple one-pot synthesis of aryl alkyl sulfides from various bromobenzenes containing a hydroxy, hydroxymethyl, hydroxyethyl, and carboxylic acid group at -o, -m, and -p positions is reported here. The reaction proceeds through, in sequence, in situ pro

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