156155-53-2 Usage
Compound Type
Diol
Functional Groups
Two hydroxyl (OH) groups
One double bond in the E configuration
Structural Features
Derived from octadiene
Two methyl groups attached at the 2,6 positions
Industrial Applications
Used in plastics manufacturing
Employed in adhesive formulations
Utilized in coatings production
Essential in the synthesis of other organic compounds
Handling Precautions
Requires careful handling
May pose health risks if mishandled
Potential environmental hazards if not managed properly
Check Digit Verification of cas no
The CAS Registry Mumber 156155-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,5 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156155-53:
(8*1)+(7*5)+(6*6)+(5*1)+(4*5)+(3*5)+(2*5)+(1*3)=132
132 % 10 = 2
So 156155-53-2 is a valid CAS Registry Number.
156155-53-2Relevant articles and documents
Investigations of the Biosynthesis of Indole Alkaloids. Feeding Experiments with Synthetic Radioactively Labelled Monoterpene Aldehydes
Battersby, Alan R.,Thompson, Mervyn,Gluesenkamp, Karl-Heinz,Tietze, Lutz-F.
, p. 3430 - 3438 (2007/10/02)
Oxidation of citral (8a/8b) with selenium oxide using different reaction conditions gave the hydroxy aldehydes 4a/4b and the dialdehydes 5a/b.Reduction of 5a/b with potassium borohydride in the presence of LiCl led to the hydroxy aldehyes 4c/d.Feeding experiments with the corresponding tritiated compounds 4a - d and 5a/b to Catharanthus roseus G.Don indicate that 4a/b, 4c/d, and 5a/b are biogenetic precursors of secologanin (3) and the indole alkaloids of the Corynanthe, Aspidosperma, and Iboga type.
