28638-29-1 Usage
Uses
Used in Food Industry:
2,3,4-Trimethyl-5-hexen-3-ol is used as a flavoring agent for its characteristic fruity and floral aroma, enhancing the taste and smell of various food products.
Used in Perfume and Cosmetics Industry:
2,3,4-TRIMETHYL-5-HEXEN-3-OL is used as a fragrance ingredient in perfumes, cosmetics, and personal care products, adding a pleasant scent and improving the sensory experience of these products.
Used in Pest Control:
2,3,4-Trimethyl-5-hexen-3-ol possesses insecticidal properties and is used as a repellent against certain pests, providing a natural alternative to chemical pesticides.
Used in Chemical Synthesis:
2,3,4-TRIMETHYL-5-HEXEN-3-OL is utilized in the synthesis of other chemicals, contributing to the production of various chemical products.
Used in Household and Industrial Products:
2,3,4-Trimethyl-5-hexen-3-ol is used as a fragrance in household and industrial products, providing a pleasant scent and improving the overall experience of using these products.
However, it is important to handle 2,3,4-trimethyl-5-hexen-3-ol with caution, as it can be irritating to the skin, eyes, and respiratory system. Proper safety measures should be taken during its use and handling to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 28638-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,3 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28638-29:
(7*2)+(6*8)+(5*6)+(4*3)+(3*8)+(2*2)+(1*9)=141
141 % 10 = 1
So 28638-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-6-8(4)9(5,10)7(2)3/h6-8,10H,1H2,2-5H3
28638-29-1Relevant academic research and scientific papers
Stereoselective Addition of Organotitanium Reagents to Carbonyl Compounds
Reetz, Manfred T.,Steinbach, Rainer,Westermann, Juergen,Peter, Roland,Wenderoth, Bernd
, p. 1441 - 1454 (2007/10/02)
Titanation of alkyllithium or -magnesium compounds using ClTi(OR)3 results in reagents which show markedly increased diastereofacial selectivity (80 - 90percent) in reactions with α-chiral aldehydes or ketones.Titanation is also the method of choice in Grignard-type additions to substituted cyclohexanones; CH3Ti(OCHMe2)3 (6a) adds predominantly from the equatorial direction, while allyltitanium reagents 11b and 12 show axial preference.Crotyltitanium compounds react with carbonyl compounds to afford primarily adducts having anti-configuration, a process which is of particular value in case of ketones (anti/syn ratios up to 99:1).Titanation of (trimethylsilyl)allyllithium (48) with Ti(OCHMe2)4 reverses regioselectivity in reactions with aldehydes and ketones, β-hydroxy silanes 50 being the only observed products.These have anti-configuration and can be converted either into Z- or E-dienes using the Peterson elimination under basic or acidic conditions, respectively.
