Detail of "126-91-0"

Reference

Preparation of linalool oxides by bioconversion

Preparation of linalool oxides by bioconversion. David, L.; Veschambre, H. (ERA 392, Univ. Clermont II, Aubiere 63170, Fr.Some commonly used reagents like 28380-24-7 and 41720-55-2 are used in this experiment.). Tetrahedron Lett., 25(5), 543-6 (French) 1984. CODEN: TELEAY. ISSN: 0040-4039. DOCUMENT TYPE: Journal CA Section: 16 (Fermentation and Bioindustrial Chemistry) Microbial cyclization of (+)linalool [126-90-9], (-)linalool [126-91-0], and (±)linalool [22564-99-4] by a nigericin [28380-24-7]-producing Streptomyces albus gives linalool oxides. cis-Linalool oxide (I) [4031-48-5] gives opposite signs for the rotatory power when measured as the pure compd. or in soln. .

Monoterpenoids as repellents against the German cockroach (Blattella germanica L

Monoterpenoids as repellents against the German cockroach (Blattella germanica L.). Inazuka, Shinichi (Kawasaki Fact., Ajinomoto Co., Kawasaki 220, Japan). Nippon Noyaku Gakkaishi, 8(3), 293-9 (Japanese) 1983. CODEN: NNGADV. ISSN: 0385-1559. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) Sixty-two monoterpenoids were tested for their repellencies toward German cockroaches by test tube and beaker methods. (-)-Linalool [126-91-0], nerol [106-25-2], (-)-carvone [6485-40-1], (+)-pulegol [22472-79-3], (+)-pulegone [89-82-7], and (+)-isopulegol [20549-46-6] had highest activities, whereas 32 other compds. including of 13 bicyclic monoterpenoids had no or very low activities. Repellency had no relationship with the volatility or the mol.There are some commonly used reagents with their cas registry numbers 6485-40-1 and 20549-46-6 in this article. size, but was related to the mol. configuration and the position of functional groups. .