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Ethanone, 1-(tetrahydro-5,5-dimethyl-2-furanyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77940-15-9

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77940-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77940-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,4 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77940-15:
(7*7)+(6*7)+(5*9)+(4*4)+(3*0)+(2*1)+(1*5)=159
159 % 10 = 9
So 77940-15-9 is a valid CAS Registry Number.

77940-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name acetyl-5 dimethyl-2,2 tetrahydrofuranne

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-5-acetyl-tetrahydrofuran

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:77940-15-9 SDS

77940-15-9Downstream Products

77940-15-9Relevant academic research and scientific papers

IMINIUM SALT ORGANOCATALYSTS, METHODS OF MAKING, AND METHODS OF USING

-

Page/Page column 37-38, (2018/04/11)

Aspects of the present disclosure include compositions comprising iminium catalyst, methods of making, methods of using, and the like.

An Iminium Salt Organocatalyst for Selective Aliphatic C-H Hydroxylation

Wang, Daoyong,Shuler, William G.,Pierce, Conor J.,Hilinski, Michael K.

supporting information, p. 3826 - 3829 (2016/08/16)

The first examples of catalysis of aliphatic C-H hydroxylation by an iminium salt are presented. The method allows the selective organocatalytic hydroxylation of unactivated 3° C-H bonds at room temperature using hydrogen peroxide as the terminal oxidant. Hydroxylation of an unactivated 2° C-H bond is also demonstrated. Furthermore, improved functional group compatibility over other catalytic methods is reported in the form of selectivity for aliphatic C-H hydroxylation over alcohol oxidation. On the basis of initial mechanistic studies, an oxaziridinium species is proposed as the active oxidant.

OXIDATION OF TETRAHYDROFURAN METHANOL DERIVATIVES WITH PYRIDINIUM CHLOROCHROMATE: A FACILE SYNTHESIS OF γ-BUTYROLACTONES

Baskaran, S.,Chandrasekaran, S.

, p. 2775 - 2778 (2007/10/02)

Treatment of a number of tetrahydrofuran methanol derivatives with pyridinium chlorochromate led to the formation of the corresponding γ-butyrolactones with the loss of one or more carbon atoms in good yields under mild reaction conditions.

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