67845-78-7 Usage
Physical state
Colorless liquid
Odor
Strong, sweet
Usage
Commonly used as a fragrance ingredient in perfumes and other personal care products
Family
Cyclohexene family (organic compounds containing a cyclohexene ring)
Production method
Reaction of cyclohexene with acetone and acetic acid
Natural occurrence
Found naturally in various plants and essential oils
Stability
Relatively stable
Toxicity
Non-toxic
Environmental impact
Low potential for environmental harm
Check Digit Verification of cas no
The CAS Registry Mumber 67845-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,4 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67845-78:
(7*6)+(6*7)+(5*8)+(4*4)+(3*5)+(2*7)+(1*8)=177
177 % 10 = 7
So 67845-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H20/c1-8(2)12-10(4)6-9(3)7-11(12)5/h6,10-12H,1,7H2,2-5H3
67845-78-7Relevant academic research and scientific papers
Cycloadditions of Allyl Cations, 27. Dehydrative Cyclodimerization of 4-Methyl-3-penten-2-ol in Two Phases. One-Pot Preparation of Dimethylated Limonenes and α-Terpineol
Vathke-Ernst, Heidrun,Hoffmann, H. M. R.
, p. 1548 - 1550 (2007/10/02)
Dehydrative Eintopfcyclodimerisierung von 4-Methyl-3-penten-2-ol (1) in einem Gemisch aus waessriger Toluolsulfonsaeure/Kohlenwasserstoff gibt dimethylierte Limonene 2a und c sowie dimethyliertes α-Terpineol 3.
