56058-69-6 Usage
Description
(E)-tetrahydro-2,2-dimethyl-5-(1-methyl-1-propenyl)furan, also known as (E)-TMTDF, is a chemical compound characterized by its molecular formula C13H22O. It is a colorless liquid with a distinctive sweet, floral odor, and is recognized for its natural occurrence in a range of foods such as coffee, cocoa, black tea, and roasted barley.
Uses
Used in the Food Industry:
(E)-tetrahydro-2,2-dimethyl-5-(1-methyl-1-propenyl)furan is used as a flavoring agent for its ability to impart a sweet, floral taste and aroma to various food products. Its natural presence in several types of food items contributes to the enhancement of their overall flavor profile.
Used in the Perfume Industry:
In the perfume industry, (E)-TMTDF is utilized as an additive to create pleasant and long-lasting scents. Its sweet, floral odor makes it a valuable component in the formulation of fragrances.
Used in Personal Care Products:
(E)-tetrahydro-2,2-dimethyl-5-(1-methyl-1-propenyl)furan is also used in the personal care sector to add a delightful scent to products such as lotions, creams, and shampoos, thereby improving the sensory experience for consumers.
Safety and Regulation:
(E)-TMTDF is considered safe for use in the food and cosmetics industries, and it is often employed to boost the flavor and scent of a wide array of products without posing any significant health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 56058-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,5 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56058-69:
(7*5)+(6*6)+(5*0)+(4*5)+(3*8)+(2*6)+(1*9)=136
136 % 10 = 6
So 56058-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-5-8(2)9-6-7-10(3,4)11-9/h5,9H,6-7H2,1-4H3/b8-5+
56058-69-6Relevant articles and documents
Regiochemical Control in the Reductive Cleavage of 2-Alkylated Oxetanes by Use of Trialkylaluminums. Tertiary Organolithiums with γ-Oxy Functionality
Mudryk, Boguslaw,Cohen, Theodore
, p. 5760 - 5761 (2007/10/02)
Whereas 2,2-dialkylated oxetanes are cleaved by lithium 4,4'-di-tert-butylbiphenylide to provide the primary organolithium-tertiary oxyanions, the same reaction in the presence of trialkylaluminums gives exclusively the 3-lithio-3,3-disubstituted propoxides, which are trapped by carbonyl compounds in moderate yields.
