1551-44-6 Usage
Chemical Properties
Cyclohexyl butyrate has a fresh, floral odor reminiscent of benzyl butyrate; and an intense, sweet taste.
Occurrence
Reported found in kumquat peel oil and passion fruit juice.
Uses
Cyclohexyl Butyrate is a synthetic flavoring agent that is a stable,
colorless liquid of fruity odor. it should be stored in glass, tin, or
resin-lined containers. it is used in pineapple, apricot, banana, and
berry flavor with applications in beverages, ice cream, and candy at
4–9 ppm.
Preparation
By esterification of cyclohexanol with isobutyric acid
Synthesis Reference(s)
Tetrahedron Letters, 31, p. 2273, 1990 DOI: 10.1016/0040-4039(90)80204-Y
Check Digit Verification of cas no
The CAS Registry Mumber 1551-44-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1551-44:
(6*1)+(5*5)+(4*5)+(3*1)+(2*4)+(1*4)=66
66 % 10 = 6
So 1551-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-2-6-10(11)12-9-7-4-3-5-8-9/h9H,2-8H2,1H3
1551-44-6Relevant articles and documents
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Simons,Meunier
, p. 1921 (1941)
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Graphite oxide as an efficient solid reagent for esterification reactions
Mirza-Aghayan, Maryam,Rahimifard, Mahshid,Boukherroub, Rabah
, p. 859 - 864 (2014/12/10)
Esterification of organic acids with alcohols under mild conditions in high yields using graphite oxide, a readily available and inexpensive material, as an effective reagent is described.
Ruthenium pincer-catalyzed cross-dehydrogenative coupling of primary alcohols with secondary alcohols under neutral conditions
Srimani, Dipankar,Balaraman, Ekambaram,Gnanaprakasam, Boopathy,Ben-David, Yehoshoa,Milstein, David
supporting information, p. 2403 - 2406 (2012/11/07)
Cross-dehydrogenative coupling of primary alcohols with secondary alcohols to obtain mixed esters with the liberation of molecular hydrogen is achieved in high yield and good selectivity under neutral conditions, using a bipyridyl-based PNN ruthenium(II) pincer catalyst. Copyright