1730-89-8 Usage
Description
(S)-(+)-4-METHYLHEXANOIC ACID, with the molecular formula C7H14O2, is a chiral compound that possesses a non-superimposable mirror image. The (S)-(+)-enantiomer is the specific form being described here. This colorless liquid exhibits a pungent odor and is widely recognized for its applications across various industries.
Uses
Used in Pharmaceutical Industry:
(S)-(+)-4-METHYLHEXANOIC ACID is used as an active pharmaceutical ingredient for its potential therapeutic properties, contributing to the development of new medications.
Used in Fragrance Industry:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a scent component for its distinctive aroma, enhancing the olfactory profiles of various fragrances.
Used in Flavoring Industry:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a flavor enhancer for its ability to impart unique taste characteristics to food and beverages.
Used in Polymer Production:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a monomer or a building block in the synthesis of polymers, contributing to the creation of materials with specific properties for various applications.
Used in Organic Synthesis:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a precursor in organic synthesis, enabling the production of a range of chemical compounds for industrial and commercial use.
Overall, (S)-(+)-4-METHYLHEXANOIC ACID is a versatile chemical compound that plays a significant role in the development and manufacturing processes across different sectors, making it an indispensable asset 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.