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(R)-3-Methylheptanoic acid

CAS No.
57403-74-4
Chemical Name:
(R)-3-Methylheptanoic acid
Synonyms
(R)-3-Methylheptanoic acid;(3R)-3-Methylheptanoic acid;Heptanoic acid, 3-methyl-, (3R)-
CBNumber:
CB6405023
Molecular Formula:
C8H16O2
Molecular Weight:
144.21
MDL Number:
MFCD04112704
MOL File:
57403-74-4.mol
Last updated:2026-09-12 18:54:14

(R)-3-Methylheptanoic acid price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ACHEMBLOCK W166165 (R)-3-methylheptanoic acid 95% 57403-74-4 100MG $465 2026-05-27 Buy
ACHEMBLOCK W166165 (R)-3-methylheptanoic acid 95% 57403-74-4 250MG $930 2026-05-27 Buy
ACHEMBLOCK W166165 (R)-3-methylheptanoic acid 95% 57403-74-4 1G $2420 2026-05-27 Buy
American Custom Chemicals Corporation CCH0006148 (R)-3-METHYLHEPTANOIC ACID 98.00% 57403-74-4 5MG $504.54 2021-12-16 Buy
Product number Packaging Price Buy
W166165 100MG $465 Buy
W166165 250MG $930 Buy
W166165 1G $2420 Buy
CCH0006148 5MG $504.54 Buy

(R)-3-Methylheptanoic acid Chemical Properties,Uses,Production

Description

(R)-3-methylheptanoic acid and (S)-3-methylheptanoic acid are a pair of chiral compounds. Their synthesis is based on the chiral methyl derivatives 3 and 4 of (R)-4-methyl-δ-pentalactone as starting materials. (R)-3-methylheptanoic acid is a component of the abdominal sex-attracting secretion of male Kheper ni groaeneus dung beetle.[1]

Definition

ChEBI: 3R-Methylheptanoic acid is a medium-chain fatty acid.

Synthesis

The synthesis of the (R)-3-METHYLHEPTANOIC ACID 2 from ester 4. Starting from the right side, reduc tion with LiAlH4 followed by Swern oxidation, allowed to convert ester 4 into aldehyde 10, which underwent Wittig olefination smoothly to provide alkene 11 in high yield. Hydrogenation of the double bond and removal of the MOM ether in 11 gave alcohol 12 whose newly ex posed hydroxyl was employed to expand one carbon. From 12, a three-step sequence involving sulfonylation (TsCl in pyridine), cyano substitution (NaCN in DMSO) and hydrolysis of nitrile (reflux in sulfuric acid/water) gave the desired (R)-methylheptanoic acid 2 over three steps in 83% yield. The enantiomer excess of 2 was measured by its derivative 15 to be 95.6%.[1]
synthesis of (R)-3-METHYLHEPTANOIC ACID

References

[1] Shunji Zhang, Weisheng T., Yong Shi. (2015). Syntheses of (R)- and (S)-3-Methylheptanoic Acids. Chinese Journal of Chemistry, 33 6, 674–678. https://doi.org/10.1002/cjoc.201400861

(R)-3-Methylheptanoic acid Preparation Products And Raw materials

Raw materials

Preparation Products

(R)-3-Methylheptanoic acid Suppliers

Global( 4)Suppliers
Supplier Tel Email Country ProdList Advantage
Tetranov Biopharm 13526569071 sales@leadmedpharm.com China 7882 64
Shandong JunRui Pharmaceutical Co., Ltd. 0539-5636807 15762008972 ffeng813@163.com China 245 58
(3R)-3-Methylheptanoic acid Heptanoic acid, 3-methyl-, (3R)- (R)-3-Methylheptanoic acid 57403-74-4