1730-89-8 Usage
General Description
(S)-(+)-4-Methylhexanoic acid is a chemical compound with the molecular formula C7H14O2. It is a chiral compound, meaning it has a non-superimposable mirror image, and the (S)-(+)-enantiomer is the specific form being described. This acid is a colorless liquid with a pungent odor, and it is commonly used in the manufacturing of pharmaceuticals, fragrances, and flavorings. It also has applications in the production of polymers and as a precursor in organic synthesis. The (S)-(+)-4-Methylhexanoic acid is an important building block in the development of various industrial and commercial products, making it a valuable chemical compound in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1730-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1730-89:
(6*1)+(5*7)+(4*3)+(3*0)+(2*8)+(1*9)=78
78 % 10 = 8
So 1730-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-3-6(2)4-5-7(8)9/h6H,3-5H2,1-2H3,(H,8,9)/t6-/m0/s1
1730-89-8Relevant articles and documents
Synthese von optisch aktiven Trogoderma-Pheromonen durch Kolbe-Elektrolyse
Jensen, Uta,Schaefer, Hans-J.
, p. 292 - 297 (2007/10/02)
The (R)-(-)-enantiomers of (Z)- (1) and (E)-14-methyl-8-hexadecen-1-ol (2) have been synthesized by coelectrolysis of (R)-(-)-4-methylhexanoic acid (7) with 12-(tetrahydro-2-pyranyloxy)-4-dodecynoic acid (8) and its subsequent hydrogenation.The acid 7 was prepared in high optical purity from (S)-(-)-citronellol (3) by conversion of the hydroxyl group to a methyl substituent and subsequent cleavage of (R)-(-)-2,6-dimethyl-2-octene (4) with ozone.By alkylation of 4-pentynoic acid (5) with 1-bromo-7-(tetrahydro-2-pyranyloxy)heptane (6) the alkynoic acid 8 was synthesized.
