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261633-13-0

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261633-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261633-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,6,3 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 261633-13:
(8*2)+(7*6)+(6*1)+(5*6)+(4*3)+(3*3)+(2*1)+(1*3)=120
120 % 10 = 0
So 261633-13-0 is a valid CAS Registry Number.

261633-13-0SDS

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 3-(2-Fluoro)phenyl-5-mercapto-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 5-(2-FLUOROPHENYL)-4H-1,2,4-TRIAZOLE-3-THIOL

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:261633-13-0 SDS

261633-13-0Downstream Products

261633-13-0Relevant articles and documents

Fluorine containing heterocyclic compounds: Synthesis of 6-substituted-2-substituted-aryl-1,2,4-triazolo[5,1-b] 1,3,5-thiadiazin-7-one derivatives

Liu, Suyou,Qian, Xuhong,Song, Gonghua,Chen, Jing,Chen, Weidong

, p. 111 - 115 (2000)

A group of heterocylic compounds of condensed triazole-thiadiazinone derivatives containing fluorine (IIIa-h) were obtained in good yields by the reactions of the corresponding 3-aryl-5-mercapto-1,2,4-triazole (IIa-d) with N-substituted-N-chloromethyl carbamoyl chloride (I) in the presence of potassium carbonate in N,N-dimethylformamide at room temperature. Cyclization of 3-(2,3,5-trifluoro-4-methoxyl)phenyl-5-mercapto-1,2,4-triazole (IIe) with I was difficult due to an intermolecular hydrogen bond of IIe. The structures of the compounds synthesized were confirmed by IR, MS, 1H NMR and elemental analyses. Fungicidal and insecticidal activities of these compounds were also studied.

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