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3613-97-6

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3613-97-6 Usage

General Description

Phenoxyacetic N,N-diethylamide is a chemical compound that belongs to the phenoxyacetamide class of chemicals. It is commonly used as a herbicide and plant growth regulator. Phenoxyacetic N,N-diethylamide works by disrupting the growth and metabolism of plants, leading to their death. This chemical is highly toxic to aquatic organisms and can cause skin and eye irritation in humans. It is important to handle phenoxyacetic N,N-diethylamide with caution and follow safety guidelines when using it in agricultural or industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 3613-97-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3613-97:
(6*3)+(5*6)+(4*1)+(3*3)+(2*9)+(1*7)=86
86 % 10 = 6
So 3613-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-3-13(4-2)12(14)10-15-11-8-6-5-7-9-11/h5-9H,3-4,10H2,1-2H3

3613-97-6SDS

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 N,N-diethyl-2-phenoxyacetamide

1.2 Other means of identification

Product number -
Other names N.N-Diaethyl-2-phenoxy-acetamid

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:3613-97-6 SDS

3613-97-6Relevant articles and documents

A practical in situ generation of the schwartz reagent. reduction of tertiary amides to aldehydes and hydrozirconation

Zhao, Yigang,Snieckus, Victor

supporting information, p. 390 - 393 (2014/04/03)

A new, highly efficient in situ protocol (Cp2ZrCl2/LiAlH(OBu-t)3) is described for the generation of the Schwartz reagent which provides a convenient method for the amide to aldehyde reduction and the regioselective hydrozirconation-iodination of alkynes and alkenes. Highlighted are chemoselective reductions of benzamides derived by directed ortho metalation (DoM) chemistry, allowing the synthesis of valuable 1,2,3-substituted benzaldehydes. The single-step, three-component process proceeds in a very short reaction time, shows excellent functional group compatibility, and uses inexpensive and long-storage stable reducing reagents.

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