Welcome to LookChem.com Sign In|Join Free

CAS

  • or

19177-72-1

Post Buying Request

19177-72-1 Suppliers

Recommended suppliersmore

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

19177-72-1 Usage

General Description

1-phenyl-3-(2,2,2-trichloro-1-hydroxyethyl)urea, also known as diuron, is a synthetic organic compound that belongs to the phenylurea herbicides group. It is widely used as a pre-emergent herbicide to control grasses and broadleaf weeds in various crops, including sugar cane, cotton, and fruit trees. Diuron works by inhibiting photosynthesis in targeted plants, disrupting their ability to produce energy from sunlight. It is classified as a low to moderate toxicity chemical and is generally considered safe for use when applied according to label instructions. However, it may pose risks to aquatic ecosystems and has been found to persist in the environment for an extended period, leading to potential concerns about bioaccumulation and long-term environmental impacts.

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 articles and documents

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

What can I do for you?
Get Best Price

Get Best Price for 19177-72-1