5370-08-1 Usage
Uses
Used in the Food Industry:
(2Z)-1,1,4,4-tetramethoxybut-2-ene is utilized as a flavoring agent for its sweet, floral scent, enhancing the taste and aroma of various food products.
Used in the Perfume Industry:
In the perfume industry, (2Z)-1,1,4,4-tetramethoxybut-2-ene serves as a fragrance component, contributing to the creation of complex and appealing scents in perfumes and other fragrance products.
Used in Chemical Synthesis:
(2Z)-1,1,4,4-tetramethoxybut-2-ene is employed in the synthesis of other organic compounds, playing a crucial role in the development of new chemical products and materials.
Used as a Reagent in Chemical Reactions:
(2Z)-1,1,4,4-tetramethoxybut-2-ene is also used as a reagent in various chemical reactions, facilitating specific transformations and processes in the chemical industry.
Used in Pharmaceutical Research:
(2Z)-1,1,4,4-tetramethoxybut-2-ene has been studied for its potential medicinal properties, including antioxidant and anti-inflammatory effects, which could lead to the development of new drugs and treatments in the future.
Check Digit Verification of cas no
The CAS Registry Mumber 5370-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5370-08:
(6*5)+(5*3)+(4*7)+(3*0)+(2*0)+(1*8)=81
81 % 10 = 1
So 5370-08-1 is a valid CAS Registry Number.
5370-08-1Relevant articles and documents
METHOD FOR PRODUCING BUTENE DIALDEHYDE-BIS-DIALKYL ACETALS
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Page/Page column 10-12, (2010/11/24)
The invention relates to a method for producing butene dialdehyde-bis-dialkyl acetals, according to which a dialkoxy dihydrofuran, an alkanol and a trialkyl orthoformiate are introduced into a rectifying column and are reacted in at least one zone of the column to form a butene dialdehyde-bis-dialkyl acetal and an alkyl formiate. The butene dialdehyde-bis-dialkyl acetal and the alkyl formiate are continuously eliminated from the reaction zone, preferably by withdrawing the alkyl formiate at the head of the column and the butene dialdehyde-bis-dialkyl acetal as a bottom product from the column. The dialkoxy dihydrofuran can be e.g. dimethoxy dihydrofuran, the alkanol can be methanol and the trialkyl orthoformiate can be trimethyl orthoformiate.
