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253686-24-7

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253686-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253686-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,8 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 253686-24:
(8*2)+(7*5)+(6*3)+(5*6)+(4*8)+(3*6)+(2*2)+(1*4)=157
157 % 10 = 7
So 253686-24-7 is a valid CAS Registry Number.

253686-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-α-fluoro-3-picoline

1.2 Other means of identification

Product number -
Other names 2-Chloro-5-fluoromethyl-pyridine

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:253686-24-7 SDS

253686-24-7Downstream Products

253686-24-7Relevant articles and documents

An efficient synthesis of (fluoromethyl)pyridylamines for labeling with fluorine-18

Lee, Kyo Chul,Chi, Dae Yoon

, p. 8576 - 8581 (1999)

We have described a two-step method for the preparation of (fluoromethyl)pyridyl-substituted amines. The sequence involves fluoride ion displacement of methanesulfonates (mesylates) of 6-chloro-α-hydroxy-2- and - 3-picolines, followed by arylation of the amine by chloropicoline. We have called this sequence fluorination-N-arylation. 1-Phenylpiperazine has been used as a model amine. Two key precursors for this sequence are the mesylates of 6-chloro-α-hydroxy-2- and -3-picolines. The former was synthesized in four steps from 6-chloro-2-picoline in 78% yield and the latter in three steps from 6-chloronicotinic acid in 53% yield. This fluorination-N-arylation sequence is sufficiently rapid and efficient for the preparation of a variety of aryl-substituted amine compounds labeled with the short half-life (t( 1/2 ) = 110 min) positron-emitting radionuclide fluorine-18.

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