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Benzenemethanol, 3-[4-(hydroxymethyl)phenoxy]-4-methoxy-, also known as 3-[4-(hydroxymethyl)phenoxy]-4-methoxybenzenemethanol, is a complex organic compound with the chemical formula C15H16O3. It is a derivative of benzenemethanol, featuring a phenoxy group at the 3-position, a hydroxymethyl group at the 4-position of the phenoxy, and a methoxy group at the 4-position of the benzene ring. Benzenemethanol, 3-[4-(hydroxymethyl)phenoxy]-4-methoxy- is characterized by its molecular weight of 244.29 g/mol and is likely to be a colorless to pale yellow solid. It may have applications in the pharmaceutical or chemical industries, potentially as an intermediate in the synthesis of more complex molecules. Due to its structure, it could exhibit specific chemical properties, such as reactivity with electrophiles or nucleophiles, depending on the context of its use.

57422-19-2

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57422-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57422-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,2 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57422-19:
(7*5)+(6*7)+(5*4)+(4*2)+(3*2)+(2*1)+(1*9)=122
122 % 10 = 2
So 57422-19-2 is a valid CAS Registry Number.

57422-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[5-(hydroxymethyl)-2-methoxyphenoxy]phenyl]methanol

1.2 Other means of identification

Product number -
Other names 4',5-Dihydroxymethyl-2-methoxydiphenylether

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:57422-19-2 SDS

57422-19-2Relevant academic research and scientific papers

Nematocidal activity of natural polyphenols from Bryophytes and their derivatives

Gamenara,Pandolfi,Saldana,Dominguez,Martinez,Seoane

, p. 506 - 510 (2007/10/03)

The nematocidal in vitro activity of three natural perrottetins (phenolic bisbibenzylethers) and eleven diphenyl ethers used as synthetic precursors has been assayed using two different experimental models, Caenorhabditis elegans and Nippostrongylus brasi

Alkylations of chiral imidazolidinones derived from di- and triglycine and attempts at cyclisations to give cycloisodityrosines

Bezencon, Olivier,Seebach, Dieter

, p. 1259 - 1276 (2007/10/03)

Di- and triglycine derivatives (1-5) containing a 2-tert-butyl-1,3-imidazolidin-4-one moiety were prepared in rac. and enantiopure forms. By deprotonations with LiNR2 these imidazolidinones were converted to Li, Li2, and Li3/su

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