Detail of "15489-27-7"

MSDS Download
CAS Number:
15489-27-7
Name:
Cuprate(2-),tetrachloro-, dilithium, (SP-4-1)- (9CI)
Molecular Structure:
Formula:
Cl4Cu . 2 Li
Molecular Weight:
219.24
Synonyms:
Cuprate(2-),tetrachloro-, dilithium (8CI); Copper lithium chloride (CuLi2Cl4); Dilithiumcopper tetrachloride; Dilithium tetrachlorocuprate; Dilithiumtetrachlorocuprate(2-)
Density:
0.91 g/mL at 25 °C
Boiling Point:
66°C
Flash Point:
1 °F
Hazard Symbols:
FXi
Risk Codes:
11-19-36/37
Safety:
16-29-33 Details
Transport Information:
UN 1993 3

Display：

Lithium tetrachlorocuprate

Verified-Platinum Supplier 2nd Year Platinum
Supplier 1585 Integral
1585

Tel:86- 022-60501183

Address:Tianjin

Molecular Formula: Cl4CuLi2 Formula Weight: 219.24 CAS No.: 15489-27-7

Supplier:SINOJIE (HK) Limited [ China (Mainland)]

610 Integral
610

Tel:+86-(0)21-52303866 / 77

Address:Room 601,Kaili Building,No.432 Huaihai Xi Road, Shanghai 200052,PRC.

Please post your buying leads,so that our qualified suppliers will soon contact you!
*Required Fields

5-Deoxy-3-O-arylmethyl or substituted arylmethyl-1,2-O-alkylidene-a-D-xylofuranose herbicide derivatives: 5-Deoxy-3-O-arylmethyl or substituted arylmethyl-1,2-O-alkylidene-a-D-xylofuranose herbicide derivatives. Loh, William (Chevron Research Co. , USA). U.S. US 4429119 A 31 Jan 1984, 19 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: C07H017-04; A01N043-08. NCL: 536181000.Several substances with their cas registry numbers 15489-27-7 and 89755-69-1 may be metioned in this study. APPLICATION: US 82-409236 18 Aug 1982. DOCUMENT TYPE: Patent CA Section: 33 (Carbohydrates) Section cross-reference(s): 5 The title compds. I [R = alkyl, alkenyl; R1 = 2-CF3C6H4, aryl, aryl substituted by alkyl, alkoxy, or halo; R2, R3 = H, alkyl] were prepd. Thus, 1,2-O-isopropylidene-a-D-xylofuranose, obtained by acetonation of D-xylose, was 5-O-tosylated and then treated with EtMgBr in the presence of Li2CuCl4 to give 1,2-O-isopropylidene-5-deoxy-5-C-ethyl-a-D-xylofuranose (II), which was benzylated with PhCH2Br to give the 3-O-benzyl deriv. of II. At 27.5 mg/cm2 application, I possessed very good pre-emergence herbicidal activity against grasses and in some instances also exhibited pre-emergence herbicidal activity against broad-leaf plants and some post-emergence activity. .

Pheromone synthesis: Pheromone synthesis.Several substances are used for example 647024-92-8 and 15489-27-7 which are their cas registry numbers. Part 222. Synthesis of the enantiomers of 21-methyl-7-hentriacontanone and a stereoisomeric mixture of 5-acetoxy-19-methylnonacosane, candidates for the female sex pheromone of the screwworm fly, Cochliomyia hominivorax. Mori, Kenji (Insect Pheromone and Traps Division, Fuji Flavor Co., Ltd., Hamura-City 205-8503, Japan). Bioscience, Biotechnology, and Biochemistry, 67(10), 2224-2231 (English) 2003 Japan Society for Bioscience, Biotechnology, and Agrochemistry. CODEN: BBBIEJ. ISSN: 0916-8451. DOCUMENT TYPE: Journal CA Section: 26 (Biomolecules and Their Synthetic Analogs) Section cross-reference(s): 12 The enantiomers of 21-methyl-7-hentriacontanone, which might show weak bioactivity as the female sex pheromone of the screwworm fly (Cochliomyia hominivorax), were synthesized by starting from the enantiomers of citronellal. (±)-Citronellol was converted to a racemic and diastereomeric mixt. of 5-acetoxy-19-methylnonacosane (I), which was considered to be a candidate for the female sex pheromone of C. hominivorax. Synthetic I exhibited no pheromone activity against male C. hominivorax. .