1017778-98-1

Basic information

• Product Name: 2-METHOXY-6-(TRIFLUOROMETHYL)BENZALDEHYDE
• Synonyms: 2-METHOXY-6-(TRIFLUOROMETHYL)BENZALDEHYDE
• CAS NO: 1017778-98-1
• Molecular Formula: C₉H₇F₃O₂
• Molecular Weight: 204.15
• Mol File: 1017778-98-1.mol

Chemical Properties

• Appearance: /
• Water Solubility: Insoluble in water.
• CAS DataBase Reference: 2-METHOXY-6-(TRIFLUOROMETHYL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXY-6-(TRIFLUOROMETHYL)BENZALDEHYDE(1017778-98-1)
• EPA Substance Registry System: 2-METHOXY-6-(TRIFLUOROMETHYL)BENZALDEHYDE(1017778-98-1)

Safety Data

• Hazardous Substances Data: 1017778-98-1(Hazardous Substances Data)

Usage

Uses

Used as catalyst in diethylzinc addition to aldehydes.

Upstream product

• 2591-86-8 N-Formylpiperidine 
• 454-90-0 3-(trifluoromethyl)anisole 
• 67-56-1 methanol 
• 60611-24-7 2-fluoro-6-(trifluoromethyl)benzaldehyde 

Relevant articles and documents

HERBICIDAL PROPYNYL-PHENYL COMPOUNDS

The present invention relates to a compound of formula (I) wherein: R1 is C1-C3alkoxy, C1-C2alkoxy-C1-C3alkoxy, C1-C2fluoroalkoxy, ethyl, n-propyl, n-butyl, cyclopropyl or ethynyl; R2 is hydrogen, ethyl, n-propyl, cyclopropyl, vinyl, ethynyl, C1-C3alkoxy, C1-C3fluoroalkyl, C1-C2fluoroalkoxy, C1-C2alkoxy-C1-C3alkoxy-, or C1fluoroalkoxy-C1-C3alkoxy-; provided that when R1 is ethyl, n-propyl, n-butyl, cyclopropyl or ethynyl, then R2 is hydrogen, ethyl, n-propyl, cyclopropyl, vinyl or ethynyl; and Y is O, S, S(O), S(O)2, N(C1-C2alkyl), N(C1-C2alkoxy), C(O), CR8R9 or -CR10R11CR12R13-; and and G, R3, R4, R5 and R6 are as defined herein; wherein the compound of formula (I) is optionally present as an agrochemically acceptable salt thereof. These compounds are suitable for use as herbicides. The invention therefore also relates to a method of controlling weeds, especially grassy monocotyledonous weeds, in crops of useful plants, comprising applying a compound of formula (I), or a herbicidal composition comprising such a compound, to the plants or to the locus thereof.

Ring-Substituted y1,2-Bis(4-hydroxyphenyl)ethylenediamine>dichloroplatinum(II) Complexes: Compounds with a Selective Effect on the Hormone-Dependent Mammary Carcinoma

dichloroplatinum(II) complexes with one substituent in the 2-position (CH3, CF3, F, Br, I: meso- and dl-1-PtCl2, meso-(3-5)-PtCl2, meso-(7 and 8)-PtCl2) or two substituents in the 2,6-position (CH3, Cl: meso-2-PtCl2, meso- and dl-6-PtCl2) in both benzene rings were synthesized and tested for estrogenic and toxic activities.Two complexes (meso-6-PtCl2 and meso-7-PtCl2) possess both effects.In comparative tests on estrogen receptor positive and negative mammary tumors in cell culture (MCF 7, ER+ and MDA-MB 231, ER-) and in animals (MXT, ER+ and MXT, ER-, mouse), meso-6-PtCl2 shows a selective effect on the estrogen receptor positive mammary carcinoma.A further increase of efficacy was achieved with the water-soluble (sulfato)platinum(II) derivative (meso-6-PtSO4).On the DMBA-induced hormone dependent mammary carcinoma of the SD rat, meso-6-PtSO4 is significantly more active than its ligand (meso-6) and cisplatin.