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10366-85-5

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10366-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10366-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,6 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10366-85:
(7*1)+(6*0)+(5*3)+(4*6)+(3*6)+(2*8)+(1*5)=85
85 % 10 = 5
So 10366-85-5 is a valid CAS Registry Number.

10366-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethyl-3-(trifluoromethyl)benzamide

1.2 Other means of identification

Product number -
Other names N,N-diethyl-3-trifluromethyl-benzamide

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:10366-85-5 SDS

10366-85-5Downstream Products

10366-85-5Relevant articles and documents

Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions

Li, Mingzong,Wang, Cong,Fang, Ping,Ge, Haibo

supporting information; experimental part, p. 6587 - 6589 (2011/06/25)

A novel Pd-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates has been realized under mild reaction conditions. This method provides an efficient access to N-mono- or N,N-disubstituted benzamides and benzoates.

Arthropod repellent pharmacophore models, compounds identified as fitting the pharmacophore models, and methods of making and using thereof

-

, (2008/06/13)

Disclosed herein is a pharmacophore model for arthropod repellent activity and methods of making and using thereof. The pharmacophore comprises two hydrophobic aliphatic functions, one aromatic function and one hydrogen bond acceptor function. The pharmacophore model was made using a test set of arthropod repellent compounds. Also disclosed are arthropod repellent compounds identified by screening databases with the pharmacophore model. Also disclosed are methods of repelling arthropods from a surface or area. Compositions and formulations comprising the compounds of the present invention as well as objects having the compounds of the present invention are disclosed.

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