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2-DIFLUOROMETHYL-PHENOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

271249-71-9

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271249-71-9 Usage

Uses

2-(Difluoromethyl)phenol is useful for preparing fungicides.

Check Digit Verification of cas no

The CAS Registry Mumber 271249-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,1,2,4 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 271249-71:
(8*2)+(7*7)+(6*1)+(5*2)+(4*4)+(3*9)+(2*7)+(1*1)=139
139 % 10 = 9
So 271249-71-9 is a valid CAS Registry Number.

271249-71-9SDS

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 2-(Difluoromethyl)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:271249-71-9 SDS

271249-71-9Downstream Products

271249-71-9Relevant academic research and scientific papers

Synthesis and evaluation of general mechanism-based inhibitors of sulfatases based on (difluoro)methyl phenyl sulfate and cyclic phenyl sulfamate motifs

Hanson, Sarah R.,Whalen, Lisa J.,Wong, Chi-Huey

, p. 8386 - 8395 (2008/02/05)

Several model mechanism-based inhibitors (MbIs) were designed and evaluated for their ability to inhibit sulfatases. The MbI motifs were based on simple aromatic sulfates, which are known to be commonly accepted substrates across this highly conserved enzyme class, so that they might be generally useful for sulfatase labeling studies. (Difluoro)methyl phenol sulfate analogs, constructed to release a reactive quinone methide trap, were not capable of irreversibly inactivating the sulfatase active site. On the other hand, the cyclic sulfamates (CySAs) demonstrated inhibition profiles consistent with an active site-directed mode of action. These molecules represent a novel scaffold for labeling sulfatases and for probing their catalytic mechanism.

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