Welcome to LookChem.com Sign In|Join Free
  • or
Acetaldehyde, (4-chlorophenoxy)-, oxime is a chemical compound derived from acetaldehyde and 4-chlorophenoxy. It is known for its herbicidal properties and is commonly used as a commercial herbicide and pesticide.

61756-69-2

Post Buying Request

61756-69-2 Suppliers

Recommended suppliers

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

61756-69-2 Usage

Uses

Used in Agricultural Industry:
Acetaldehyde, (4-chlorophenoxy)-, oxime is used as a herbicide for controlling weeds in agricultural settings. It is applied to crops to prevent unwanted plant growth, ensuring a more efficient and productive agricultural yield.
Used in Pesticide Formulations:
Acetaldehyde, (4-chlorophenoxy)-, oxime is used as a pesticide ingredient to manage pest populations in various agricultural and horticultural applications. Its effectiveness in controlling pests contributes to the protection of crops and plants from damage.

Check Digit Verification of cas no

The CAS Registry Mumber 61756-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,5 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61756-69:
(7*6)+(6*1)+(5*7)+(4*5)+(3*6)+(2*6)+(1*9)=142
142 % 10 = 2
So 61756-69-2 is a valid CAS Registry Number.

61756-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name p-chlorophenoxyacetaldoxime

1.2 Other means of identification

Product number -
Other names -

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:61756-69-2 SDS

61756-69-2Relevant academic research and scientific papers

Synthesis and Antitubercular Activity of 4-(5-Nitro-2-furyl/2-pyrazinyl/1-adamantyl)-2-(alkyl/aryl/arylamino)thiazoles

Khadse, B. G.,Lokhande, S. R.,Bhamaria, R. P.,Prabhu, S. R.

, p. 856 - 860 (2007/10/02)

The reaction of haloketones, obtained from Arndt-Eistert reaction on the acid chlorides of 1-adamantane, 5-nitrofuroic acid and pyrazine-2-carboxylic acid, with different thioamides and thioureas affords the title thiazoles (I-III).Some of them exhibit interesting antitubercular activity at 6.25 to 0.38 μg/ml concentration against H37Rv strain of M. tubercolosis in vitro testing.The structure activity relationship (SAR) has also been discussed.

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 61756-69-2