58609-72-6 Usage
Description
2-(4-isobutylphenyl)propionaldehyde oxime is a synthetic chemical compound known for its floral and sweet scent. It is commonly used as a fragrance ingredient in various consumer products, including perfumes, soaps, and lotions. 2-(4-isobutylphenyl)propionaldehyde oxime is designed to impart a pleasant aroma to personal care and household products, enhancing the sensory experience for users.
Uses
Used in Personal Care Industry:
2-(4-isobutylphenyl)propionaldehyde oxime is used as a fragrance ingredient for its floral and sweet scent, adding a pleasant aroma to products such as perfumes, soaps, and lotions. It helps create an enjoyable and memorable sensory experience for consumers.
Used in Household Products Industry:
In addition to personal care products, 2-(4-isobutylphenyl)propionaldehyde oxime is also used as a fragrance ingredient in household products. Its floral and sweet scent contributes to creating a more pleasant and inviting atmosphere in the home, making everyday tasks more enjoyable.
Check Digit Verification of cas no
The CAS Registry Mumber 58609-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58609-72:
(7*5)+(6*8)+(5*6)+(4*0)+(3*9)+(2*7)+(1*2)=156
156 % 10 = 6
So 58609-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H19NO/c1-10(2)8-12-4-6-13(7-5-12)11(3)9-14-15/h4-7,9-11,15H,8H2,1-3H3/b14-9+
58609-72-6Relevant articles and documents
Stereospecific 1,4-Metallate Shift Enables Stereoconvergent Synthesis of Ketoximes
Yang, Kai,Zhang, Feng,Fang, Tongchang,Zhang, Guan,Song, Qiuling
supporting information, p. 13421 - 13426 (2019/08/20)
Reported herein is a stereospecific 1,4-metallate rearrangement for single-geometry ketoxime synthesis from oxime chlorides and arylboronic acids. This strategy exhibits broad substrate scope with excellent stereoselectivity under mild reaction conditions. In comparison with the conventional approaches, each configuration of unsymmetric diaryl oximes, as well as the thermodynamically less stable Z isomer of aryl alkyl ketoximes can be selectively and exclusively obtained. The reactivities of unsymmetric diaryl oximes and the Z isomer of aryl alkyl oximes, a class of underexplored molecules, enables efficient access to the corresponding isoquinolines, isoquinoline N-oxides, and amides having a single configuration.
