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68223-64-3

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68223-64-3 Usage

Uses

4-Fluorocyclohexanone is a reactant in the synthetic preparation of rapamycin.

Check Digit Verification of cas no

The CAS Registry Mumber 68223-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,2 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68223-64:
(7*6)+(6*8)+(5*2)+(4*2)+(3*3)+(2*6)+(1*4)=133
133 % 10 = 3
So 68223-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H9FO/c7-5-1-3-6(8)4-2-5/h5H,1-4H2

68223-64-3SDS

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 4-Fluorocyclohexanone

1.2 Other means of identification

Product number -
Other names 4-fluorocyclohexan-1-one

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:68223-64-3 SDS

68223-64-3Relevant articles and documents

Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor

González-Esguevillas, María,Miró, Javier,Jeffrey, Jenna L.,MacMillan, David W.C.

supporting information, p. 4222 - 4227 (2019/06/13)

Herein we disclose a deoxyfluorination of alcohols with an electrophilic fluorine source via visible-light photoredox catalysis. This radical-mediated C–F coupling is capable of fluorinating secondary and tertiary alcohols efficiently, complementing previously reported nucleophilic deoxyfluorination protocols.

NEW BICYCLIC THIOPHENYLAMIDE COMPOUNDS

-

, (2014/01/09)

The invention provides novel compounds having the general formula (I) wherein R1, R2, R3, R4, R5, R6, R7, A, E and n are as described herein, compositions including the compounds and use thereof as fatty-acid binding protein (FABP) 4/5 inhibitors in the treatment of e.g. type 2 diabetes, atherosclerosis or cancer.

Benzamide derivatives and uses related thereto

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Page/Page column 52, (2008/06/13)

Benzamide derivatives of formulae I and II, and pharmaceutically acceptable salts, solvates, stereoisomers, and prodrugs thereof, and pharmaceutical compositions comprising the same, are described and have therapeutic utility, particularly in the treatment of diabetes, obesity, and related conditions and disorders: wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, and R12 are defined as provided herein.

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