31147-36-1 Usage
Description
(2E,6E)-1,1'-oxybis[3,7-dimethylocta-2,6-diene], also known as Oxybis, is a colorless to pale yellow liquid with a fruity, floral odor. It is a chemical compound belonging to the family of unsaturated alcohols and is commonly used as a fragrance ingredient in various consumer products.
Uses
Used in Fragrance Industry:
Oxybis is used as a fragrance ingredient for its fruity, floral odor in a wide range of consumer products, including perfumes, soaps, and lotions.
Used in Flavor and Fragrance Production for Food and Beverages:
Oxybis is used in the production of flavors and fragrances for food and beverages, enhancing the sensory experience of these products.
Used as an Intermediate in Organic Synthesis:
Oxybis can be used as an intermediate in the synthesis of other organic compounds, contributing to the development of new chemical products.
Safety:
Oxybis is generally considered to be a safe and low-toxicity chemical. However, its potential for skin irritation and sensitization are the primary concerns associated with its use, necessitating proper handling and precautions during application.
Check Digit Verification of cas no
The CAS Registry Mumber 31147-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,4 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31147-36:
(7*3)+(6*1)+(5*1)+(4*4)+(3*7)+(2*3)+(1*6)=81
81 % 10 = 1
So 31147-36-1 is a valid CAS Registry Number.
31147-36-1Relevant articles and documents
Brieger,Ellis
, p. 335,336 (1975)
Reaction of orthoesters with alcohols in the presence of acidic catalysts: A study
Sampath Kumar,Joyasawal, Sipak,Reddy,Pawan Chakravarthy,Krishna,Yadav
, p. 1686 - 1692 (2007/10/03)
Allylic and benzylic alcohols are converted into corresponding unsymmetrical ethers when reacted with various orthoesters in the presence of montmorillonite KSF at ambient temperature. A detailed study has been undertaken to examine the mechanism and generality of these reactions with regard to various acidic catalysts, which reveal interesting competitive reactions mainly O-acetylation, together with trace amount of dimerized product. The type of the side product and their relative quantity depends upon the nature of the catalyst employed. Furthermore, the low yields of the Claisen rearrangement product obtained from allylic alcohols under heating is rationalized due to the formation of some of these products.
PRENYLATION OF OLEFINS IN NITROMETHANE
Julia, M.,Schmitz, C.
, p. 2485 - 2490 (2007/10/02)
The prenylation of isopentenyl and 3,3-dimethylallyl derivatives could be achieved efficiently with dimethyl vinyl carbinol and a variety of acids in nitromethane.Geraniol and isopentenylacetate led to farnesyl derivatives.
