27944-79-2 Usage
General Description
2,4-dimethylpentanal is an organic compound with the chemical formula C7H14O. It is a colorless liquid with a strong, pungent odor and is commonly used as a flavoring agent in the food industry. It is a branched chain aldehyde, meaning it contains a carbon chain with a branching offshoot, and it is named for the two methyl groups attached to the fourth carbon in the chain. 2,4-dimethylpentanal is primarily used in the production of fragrances and perfumes, as well as in the synthesis of various chemical compounds. It is also used as a solvent and as an intermediate in the manufacture of other organic compounds. As with all chemicals, proper handling and storage procedures should be followed to ensure safety and prevent potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 27944-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,4 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27944-79:
(7*2)+(6*7)+(5*9)+(4*4)+(3*4)+(2*7)+(1*9)=152
152 % 10 = 2
So 27944-79-2 is a valid CAS Registry Number.
27944-79-2Relevant articles and documents
MANUFACTURING METHOD FOR THE ALDEHYDE BY HYDROFORMYLATION REACTION
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Paragraph 0079-0081; 0083-0084; 0101, (2021/07/13)
A phosphine ligand represented by chemical formula 1. Transition metal catalyst A hydroformylation catalyst composition comprising a solvent and a solvent. Provided is a process for preparing aldehydes by hydroformylation using olefinic compounds and formaldehyde to produce aldehydes.
ADDITION RADICALAIRE DU PROPANAL A DIVERS ALCENES ET CYCLENES : ASPECTS STERIQUES ET POLAIRES
Tabbaa, I.,Cazaux, M.,Lalande, R.
, p. 1011 - 1018 (2007/10/02)
Free radical addition of propanal to double bonds, initiated by benzoyl peroxide, mainly leads to two adducts, an aldehyde and a ketone, when the double bond has a methylene group ; these results are explained in terms of polar effects in the free radical transfert reactions.When the double bond has no methylene group, only the ketonic adduct is obtained ; the steric effects in the free radical addition step explain these results.
