16630-91-4 Usage
Description
2-Methylheptan-1-al, also known as 2-methylheptanal, is an organic compound belonging to the aldehyde family. It is characterized by a straight carbon chain with seven carbon atoms, where one of the carbons has a methyl group attached to it. 2-methylheptan-1-al has a distinct aldehyde functional group (-CHO) at the terminal end, which gives it its unique chemical properties and reactivity.
Uses
Used in Chemical Synthesis:
2-Methylheptan-1-al is used as a reagent in the field of chemical synthesis, particularly for hydroxynitrile lyase-catalyzed enzymic nitroaldol (Henry) reactions. Its aldehyde group plays a crucial role in these reactions, allowing for the formation of various organic compounds with potential applications in pharmaceuticals, agrochemicals, and other industries.
Used in Flavor and Fragrance Industry:
2-Methylheptan-1-al is also utilized in the flavor and fragrance industry due to its distinct and pleasant odor. It can be used to create a wide range of scents for perfumes, colognes, and other fragrance products, as well as to enhance the flavor of various food items.
Used in Research and Development:
In the research and development sector, 2-methylheptan-1-al serves as a valuable compound for studying the properties and reactivity of aldehydes. It can be used to investigate various chemical reactions, mechanisms, and the development of new synthetic methods and techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 16630-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,3 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16630-91:
(7*1)+(6*6)+(5*6)+(4*3)+(3*0)+(2*9)+(1*1)=104
104 % 10 = 4
So 16630-91-4 is a valid CAS Registry Number.
InChI:InChI=1S/C8H16O/c1-3-4-5-6-8(2)7-9/h7-8H,3-6H2,1-2H3
16630-91-4Relevant articles and documents
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Heilbron,Jones,McCombie
, p. 136 (1944)
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Methyl-modified cage-type phosphorus ligand and preparation method thereof Preparation method and application thereof
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Paragraph 0075-0084; 0087-0088, (2021/09/15)
The invention discloses a methyl-modified cage-type phosphorus ligand, a preparation method and application thereof, in particular to a synthesis design, wherein methyl is further introduced on a phenyl ring of triphenylphosphine, and a methyl-modified cage-type phosphorus ligand is synthesized, and when a methyl meta-substituted cage-type phosphorus ligand is used as a hydroformylation reaction catalyst the proportion of n-structural aldehyde and isomeric aldehyde is 2.6. TOF-1 The methyl-substituted cage-type phosphorus ligand is excellent in performance, stable in property and recyclable, has excellent substrate applicability in the hydroformylation catalytic reaction, has a good industrial application prospect, and has very important significance in metal organic catalysis.
Encapsulated liquid nano-droplets for efficient and selective biphasic hydroformylation of long-chain alkenes
Zhang, Xiaoli,Wei, Juan,Zhang, Xiaoming
supporting information, p. 14134 - 14138 (2019/09/18)
Aqueous nano-droplets of homogeneous Rh-TPPTS catalyst encapsulated within the cavity of hollow silica nanospheres were fabricated for biphasic hydroformylation of long-chain alkenes, which showed significant reaction rate enhancement effects and improved aldehyde selectivity.
