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1126-91-6

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1126-91-6 Usage

General Description

1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-one is a chemical compound with the molecular formula C10H16O2. It is a bicyclic ketone with an oxygen atom bridging two carbon atoms, and three methyl groups attached to the second carbon of the bicyclic ring. 1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-one is commonly used as a fragrance ingredient in perfumes and other personal care products due to its pleasant and floral odor. It is also used in the manufacturing of flavorings and as a solvent in chemical processes. Additionally, it has potential applications in the pharmaceutical industry as a building block for the synthesis of new drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 1126-91-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1126-91:
(6*1)+(5*1)+(4*2)+(3*6)+(2*9)+(1*1)=56
56 % 10 = 6
So 1126-91-6 is a valid CAS Registry Number.

1126-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,8,8-trimethyl-4-oxabicyclo[3.2.1]octan-3-one

1.2 Other means of identification

Product number -
Other names O-Butyryl-acetessigsaeure-aethylester

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:1126-91-6 SDS

1126-91-6Relevant articles and documents

Selective anodic oxidation of camphor

Ye,Beck

, p. 5463 - 5470 (2007/10/02)

Camphor (1) was anodically oxidized at Pb/PbO2 and Pt in 1M H2SO4 (50 Vol.% MeCN). 1,2-campholide (4) as the main product was obtained with material yields up to 96% and current efficiencies up to 39% at the PbO2 anode. The most important side products were oxygen and 1,8,8-trimethyl-2-oxa-bicyclo[3.3.0]octan-3-one (5). A quantitative conversion of 4 to 5 is possible in strong acids. The effects of current densities and concentrations were studied in detail.

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