Welcome to LookChem.com Sign In|Join Free
  • or
1-phenyl-3-(2,2,2-trichloro-1-hydroxyethyl)urea, commonly known as diuron, is a synthetic organic compound that is a member of the phenylurea herbicides group. It is characterized by its ability to inhibit photosynthesis in targeted plants, thereby disrupting their energy production from sunlight.

19177-72-1

Post Buying Request

19177-72-1 Suppliers

Recommended suppliers

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

19177-72-1 Usage

Uses

Used in Agricultural Industry:
1-phenyl-3-(2,2,2-trichloro-1-hydroxyethyl)urea is used as a pre-emergent herbicide for controlling grasses and broadleaf weeds in various crops such as sugar cane, cotton, and fruit trees. Its application helps in managing unwanted plant growth, thereby enhancing crop productivity and quality.
As a herbicide, diuron is effective due to its mode of action which involves inhibiting photosynthesis in the targeted plants. This action disrupts the plants' ability to convert sunlight into energy, leading to their eventual death. However, its classification as a low to moderate toxicity chemical suggests that it is generally considered safe for use when applied according to label instructions. Nonetheless, there are environmental concerns associated with diuron, particularly its potential to persist in the environment for a long time, posing risks to aquatic ecosystems and possibly leading to bioaccumulation and long-term impacts on the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 19177-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,7 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19177-72:
(7*1)+(6*9)+(5*1)+(4*7)+(3*7)+(2*7)+(1*2)=131
131 % 10 = 1
So 19177-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Cl3N2O2/c10-9(11,12)7(15)14-8(16)13-6-4-2-1-3-5-6/h1-5,7,15H,(H2,13,14,16)

19177-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-(2,2,2-trichloro-1-hydroxyethyl)urea

1.2 Other means of identification

Product number -
Other names N-Phenyl-N'-(2,2,2-trichlor-1-hydroxy-aethyl)-harnstoff

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:19177-72-1 SDS

19177-72-1Relevant academic research and scientific papers

INTRA VS INTERMOLECULAR AMIDOALKILATION OF AROMATICS

Ishai, D. Ben,Sataty, I.,Peled, N.,Goldshare, R.

, p. 439 - 450 (2007/10/02)

Three tipes of intramolecular amidoalkylation reactions of aromatics, two endotrigonal and one exotrigonal (I, II, III), leading to indolone, N-acylisoquinolines, isoquinolone and benzazepinone derivatives were studied.In the presence of external aromatic nucleophiles competing intermolecular amidoalkylations were observed (1->2, 13->14).The mechanism and the synthetic limitations of the three types of cyclization is 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 19177-72-1