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Cyclohexanone, 2-fluoro-3,3,5,5-tetramethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37783-39-4

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37783-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37783-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,8 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37783-39:
(7*3)+(6*7)+(5*7)+(4*8)+(3*3)+(2*3)+(1*9)=154
154 % 10 = 4
So 37783-39-4 is a valid CAS Registry Number.

37783-39-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-3,3,5,5-tetramethylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-Flour-3,3,5,5-tetramethyl-cyclohexanon (Flour equatorial)

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:37783-39-4 SDS

37783-39-4Downstream Products

37783-39-4Relevant academic research and scientific papers

Direct α-fluorination of ketones using N-F reagents

Stavber, Stojan,Jereb, Marjan,Zupan, Marko

, p. 2609 - 2615 (2007/10/03)

The use of 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Accufluor NFTh) as a fluorine atom transfer reagent and methanol as solvent enabled direct regiospecific fluorofunctionalization of the α-carbonyl position in ketones w

Electrolytic Partial Fluorination of Organic Compounds. 17. Regiospecific Anodic Fluorination of Sulfides Bearing Electron-Withdrawing Substituents at the Position α to the Sulfur Atom

Fuchigami, Toshio,Shimojo, Moriyasu,Konno, Akinori

, p. 3459 - 3464 (2007/10/02)

Regiospecific monofluorination of various sulfides bearing electron-withdrawing substituents, cyano, ester, acyl, amino, and phosphonate groups, at their α-positions was successfully carried out by the anodic oxidation of the sulfides in Et3N*3HF/MeCN usi

Fluorination of carbanions with N-fluoro-N-alkylsulfonamides

-

, (2008/06/13)

Process for fluorinating an organic carbanion, which process comprises contacting and reacting, in a dry inert atmosphere, the compound of the formula selected from STR1 wherein STR2 is the carbanion, M is a counter ion, and X is a halide and a selected N-flouro-N-alkylsulfonamide.

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