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Benzoic acid, 2-[(4-fluorophenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13420-72-9

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13420-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13420-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,2 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13420-72:
(7*1)+(6*3)+(5*4)+(4*2)+(3*0)+(2*7)+(1*2)=69
69 % 10 = 9
So 13420-72-9 is a valid CAS Registry Number.

13420-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-fluorophenyl)sulfanylbenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-[(4-fluorophenyl)thio]

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:13420-72-9 SDS

13420-72-9Relevant academic research and scientific papers

Regioselective copper-catalyzed C-N and C-S bond formation using amines, thiols and halobenzoic acids

Liu, Shuanglong,Pestano, John Paul C.,Wolf, Christian

, p. 3519 - 3527 (2008/09/19)

A regioselective method for highly efficient C-N and C-S bond formation with 2-halobenzoic acids is described. The Cu/Cu2O-catalyzed reaction is carried out in 2-ethoxyethanol or ethylene glycol diethyl ether and does not require the use of strong base or other additives. This procedure eliminates the need for acid protection, tolerates a wide range of functional groups and provides aromatic and aliphatic amines and sulfides in 81-99% yield. Georg Thieme Verlag Stuttgart.

Phenylthiophenylpiperidines

-

, (2008/06/13)

Novel phenylthiophenylpiperidines and methods of preparing same are described. These compounds are useful as analgetics, antidepressants, anticonvulsants and intermediates for preparing other pharmaceutically active compounds.

Spiro[dibenz(b,f)thiepin-piperidine]s

-

, (2008/06/13)

Novel spiro[dibenz(b,f)thiepin-piperidine]s and methods of preparing same are described. These compounds are useful as analgetics, tranquilizers and anticonvulsants.

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