Welcome to LookChem.com Sign In|Join Free
  • or
BUTROXYDIM is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138164-12-2

Post Buying Request

138164-12-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

138164-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138164-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,6 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138164-12:
(8*1)+(7*3)+(6*8)+(5*1)+(4*6)+(3*4)+(2*1)+(1*2)=122
122 % 10 = 2
So 138164-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H33NO4/c1-7-10-19(26)23-15(5)11-14(4)22(16(23)6)17-12-20(27)24(21(28)13-17)18(8-2)25-29-9-3/h11,17,27H,7-10,12-13H2,1-6H3/b25-18+

138164-12-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name butroxydim

1.2 Other means of identification

Product number -
Other names 2-[1-(ethoxyimino)propyl]-3-hydroxy-5-[2,4,6-trimethyl-3-(1-oxobutyl)phenyl]-2-cyclohexen-1-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:138164-12-2 SDS

138164-12-2Downstream Products

138164-12-2Relevant academic research and scientific papers

Butachlor derivative and synthesis method thereof

-

Paragraph 0011; 0032-0034; 0049-0051, (2021/02/10)

The invention discloses a butachlor derivative and a synthetic method thereof. The preparation method comprises the following steps: 1, taking a compound I as a reaction initiator, taking aluminum trichloride as a catalyst, reacting with butyryl chloride to obtain an intermediate II; 2, taking trichloromethane as a reaction solvent, and reacting with hydrogen chloride gas to obtain a correspondingderivative III; or reacting the intermediate II with dimethyl sulfate in dichloromethane or trichloromethane under an alkaline condition to obtain a corresponding derivative IV. The butachlor derivative disclosed by the invention has the advantage of inhibiting ryegrass which generates resistance to butachlor. The synthesis method provided by the invention has the advantages of safety, environmental protection, high yield, easiness in operation and the like.

Compound herbicide and preparation method thereof

-

Paragraph 0034-0036; 0052-0054, (2021/02/13)

The invention discloses a compound herbicide, which is prepared from a butroxydim derivative, ipfencarbazone, nitrophenol and carbamic acid. The invention also discloses a preparation method of the compound herbicide. According to the invention, the butroxydim derivative has the advantage of inhibiting ryegrass which generates resistance to butroxydim, and a compound herbicide obtained by compounding the butroxydim derivative with the ipfencarbazone and the carbamic acid is more excellent in weeding performance; and research results finds that the combination of the two different butroxydim derivatives has a better effect.

NOXIOUS ARTHROPOD CONTROL AGENT CONTAINING AMIDE COMPOUND

-

, (2017/08/26)

An object of the present invention is to provide a compound having the controlling activity on a noxious arthropod, and a noxious arthropod controlling agent containing an amide compound of formula (I): wherein X represents a nitrogen atom or a CH group, p represents 0 or 1, A represents a tetrahydrofuranyl group or the like, R1, R2, R3, R4, R5, R6 and R7 represent a hydrogen atom or the like, n represents 1 or 2, Y represents an oxygen atom or the like, m represents any integer of 0 to 7, and Q represents a C1-8 chain hydrocarbon group optionally having a phenyl group or the like, has the excellent noxious arthropod controlling effect.

Herbicidal mixtures having a synergistic effect

-

, (2008/06/13)

PCT No. PCT/EP96/03996 Sec. 371 Date Feb. 17, 1998 Sec. 102(e) Date Feb. 17, 1998 PCT Filed Sep. 12, 1996 PCT Pub. No. WO97/10714 PCT Pub. Date Mar. 27, 1997A composition comprising at least one sulfonylurea of the formula I wherein R1 is substituted alkyl; halogen; a group ER6 (E=O, S or NR7); COOR8; NO2; S(O)oR9; SO2NR10R11; or CONR10R11; R2 is hydrogen, alkyl, alkenyl, alkynyl, halogen, alkoxy, haloalkoxy, haloalkyl, alkylsulfonyl, nitro, cyano or alkylthio; R3 is F, CF3, CF2Cl, CF2H, OCF3, OCF2Cl, or, if R1 is CO2CH3 and R2 is simultaneously fluorine, R3 is Cl, or, if R1 is CH2CF3 or CF2CF3, R3 is methyl, or, if R4 is OCF3 or OCF2Cl, R3 is OCF2H or OCF2Br; R4 is alkoxy, alkyl, alkylthio, alkylamino, dialkylamino, halogen, haloalkyl or haloalkoxy; and R5 is hydrogen, alkoxy or alkyl; or an enviromentally compatible salt of I, and an aryloxyalkanoic acid selected from the group consisting of 2,4-D, 2,4-DB, clomeprop, dichlorprop, dichlorprop-P, dichlorprop-P (2,4-DP-P), fenoprop (2,4,5-TP), fluoroxypyr, MCPA, MCPB, mecoprop, mecoprop-P, napropamide, napropanilide, triclopyr, and an enviromentally compatible salt thereof exhibits a synergistic herbicidal effect.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 138164-12-2