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561304-41-4

561304-41-4

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561304-41-4 Usage

Chemical Properties

white powder

Check Digit Verification of cas no

The CAS Registry Mumber 561304-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,1,3,0 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 561304-41:
(8*5)+(7*6)+(6*1)+(5*3)+(4*0)+(3*4)+(2*4)+(1*1)=124
124 % 10 = 4
So 561304-41-4 is a valid CAS Registry Number.

561304-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-3-(Trifluoromethoxy)Benzoic Acid

1.2 Other means of identification

Product number -
Other names 2-AMINO-3-(TRIFLUOROMETHOXY)BENZOIC ACID

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:561304-41-4 SDS

561304-41-4Downstream Products

561304-41-4Relevant articles and documents

Design, synthesis and insecticidal activities of novel anthranilic diamides containing fluorinated groups as potential ryanodine receptors activitors

Wu, Chang-Chun,Wang, Bao-Lei,Liu, Jing-Bo,Wei, Wei,Li, Yu-Xin,Liu, Yang,Chen, Ming-Gui,Xiong, Li-Xia,Yang, Na,Li, Zheng-Ming

supporting information, p. 1248 - 1251 (2017/06/19)

In order to search for novel potent and environmentally benign insecticides, a series of anthranilic diamides containing various fluorinated groups were designed and synthesized. Their structures were confirmed by 1H NMR, 13C NMR, s

Trifluoromethoxy substituted anilines: Metalation as the key step for structural elaboration

Leroux, Frederic,Castagnetti, Eva,Schlosser, Manfred

, p. 4693 - 4699 (2007/10/03)

Trifluoromethoxy-substituted anilines undergo hydrogen/lithium permutation ("metalation") with optional site selectivity depending on the N-protective group employed. N-tert-Butoxycarbonyl-2-and -4-(trifluoromethoxy)aniline react with tert-butyllithium at

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