2307-49-5

Basic information

• Product Name: Tricamba(content>60%)
• Synonyms: Tricamba(content>60%);Metriben;3,5,6-trichloro-o-anisic acid;tricamba;Benzoic acid, 2,3,5-trichloro-6-methoxy- (9CI);Banvel T;V58-CS-25;Velsicol 58-CS-25
• CAS NO: 2307-49-5
• Molecular Formula: C₈H₅Cl₃O₃
• Molecular Weight: 255.4825
• EINECS: 218-985-2
• Mol File: 2307-49-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: 138°C
• Boiling Point: 361.82°C (rough estimate)
• Flash Point: 167.5°C
• Appearance: /
• Density: 1.6048 (rough estimate)
• Vapor Pressure: 1.33E-05mmHg at 25°C
• Refractive Index: 1.4700 (estimate)
• CAS DataBase Reference: Tricamba(content>60%)(CAS DataBase Reference)
• NIST Chemistry Reference: Tricamba(content>60%)(2307-49-5)
• EPA Substance Registry System: Tricamba(content>60%)(2307-49-5)

Safety Data

• Hazardous Substances Data: 2307-49-5(Hazardous Substances Data)

Usage

Uses

Tricamba is an antiparasitic agent. A herbicide.

Safety Profile

Poison by ingestion. When heatedto decomposition it emits toxic fumes of Clí. Used as anherbicide.

InChI:InChI=1/C8H5Cl3O3/c1-14-7-4(10)2-3(9)6(11)5(7)8(12)13/h2H,1H3,(H,12,13)

Upstream product

• 14386-55-1 methyl 2,3,5-trichloro-2 methoxybenzoate 
• 40932-60-3 3,5,6-Trichloro-2-hydroxybenzoic acid 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 69954-01-4 2,3,5-trichloro-6-methoxybenzoic acid chloride 

Relevant articles and documents

Fluorine analogs of dicamba and tricamba herbicides; Synthesis and their pesticidal activity

Fluorine analogs of the dicamba and tricamba herbicides were synthesized. Their herbicide activities were compared with the activities of the pattern herbicides dicamba and tricamba.

A cyclotrimethoxone-substituted salicylate compound and anti-tumor effect thereof

The invention relates to the technical field of medicines, and designs and synthesizes a novel A cyclotrimethoxy 4'-hydroxyflavone compound and an A cyclotrimethoxone-substituted salicylate compound. The figure 1 is a general formula of the A cyclotrimethoxone-substituted salicylate compound, wherein in the formula, R1, R2 and R3 are equal to OCH3 or R2, R3 and R4 are equal to OCH3; R5- is equal to OCH3, CH3, F, Cl, Br, I or the like. The novel A cyclotrimethoxy 4'-hydroxyflavone compound and the A cyclotrimethoxone-substituted salicylate compound can have an obvious inhibiting effect on MGC-803 (human gastric carcinoma cells), HepG2 (human hepatoma carcinoma cells), MCF-7 (human breast cancer cells) and hopefully become anti-tumor drugs. The invention discloses a preparation method of the novel A cyclotrimethoxy 4'-hydroxyflavone compound and the A cyclotrimethoxone-substituted salicylate compound.

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides of the formula STR1 where R1 is hydrogen, a metal atom or an unsubstituted or substituted ammonium radical, R2 is a saturated or unsaturated straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical or 3 to 7 carbon atoms, a branched saturated or unsaturated aliphatic radical of 3 to 10 carbon atoms, a halogen-, alkoxy- or alkylmercapto-substituted aliphatic radical of 2 to 10 carbon atoms tetrahydrofuryl substituted methyl, a cycloalkoxy-substituted aliphatic radical of 4 to 10 carbon atoms, unsubstituted or halogen-substituted benzyl or phenyl, halophenyl, or alkylphenyl of a total of up to 10 carbon atoms, R3 is hydrogen, a straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical of 3 to 7 carbon atoms, a branched aliphatic radical of 3 to 10 carbon atoms, haloalkyl, or alkoxyalkyl of 2 to 10 carbon atoms and X is oxygen and may also be sulfur if R2 is unsubstituted or halogen-substituted benzyl, processes for their preparation, and herbicides containing the above compounds.