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198879-38-8

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198879-38-8 Usage

Structure

A phenol derivative with a fluorophenylamino-methyl group attached to the aromatic ring

Potential Applications

Pharmaceutical and organic synthesis
Drug discovery and development
Basic research in organic chemistry and medicinal chemistry

Handling Precautions

It is important to handle this chemical with care and according to proper safety protocols, as it may have potential hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 198879-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,8,7 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 198879-38:
(8*1)+(7*9)+(6*8)+(5*8)+(4*7)+(3*9)+(2*3)+(1*8)=228
228 % 10 = 8
So 198879-38-8 is a valid CAS Registry Number.

198879-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-{[(4-Fluorophenyl)amino]methyl}phenol

1.2 Other means of identification

Product number -
Other names -

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:198879-38-8 SDS

198879-38-8Downstream Products

198879-38-8Relevant articles and documents

Synthesis and characterization of new 3,4-dihydro-2H-benzoand naphtho-1,3-oxazine derivatives

Gabbas, A. U. Garin,Ahmad,Zainuddin,Ibrahim

, p. 1304 - 1306 (2016)

New 1,3-benzoxazine and naphthoxazine monomers were synthesized using a modified step-wise technique in which formaldehyde was replaced with methylene bromide for ring-closure reaction in the last synthetic step. Salicylaldehyde and 2-hydroxy-1-naphthalde

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