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709-62-6

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709-62-6 Usage

Physical form

White crystalline powder

Solubility

Soluble in organic solvents

Uses

Building block in the synthesis of pharmaceutical compounds and agrochemicals, ligand in organometallic chemistry, stabilizer for polymers and plastic materials

Importance

Versatile and important intermediate in various industrial applications

Hazards

May pose hazards to human health and the environment if not handled and stored properly.

Check Digit Verification of cas no

The CAS Registry Mumber 709-62-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 709-62:
(5*7)+(4*0)+(3*9)+(2*6)+(1*2)=76
76 % 10 = 6
So 709-62-6 is a valid CAS Registry Number.

709-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-bis(trifluoromethyl)-1H-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 3,5-Bis(trifluoromethyl)-1,2,4-triazole

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:709-62-6 SDS

709-62-6Upstream product

709-62-6Relevant articles and documents

Unsaturated nitrogen compounds containing fluorine. Part 16. The synthesis of 3,5-bis(trifluoromethyl)-1H-1,2,4- triazole and some 4-substituted derivatives from 2,5-dichloro-1,1,1,6,6,6-hexafluoro-3,4-diazahexa-2,4-diene

Abdul-Ghani, Mohammad M.,Tipping, Anthony E.

, p. 95 - 106 (2007/10/02)

The dichloroazine 5 has been converted into the monoaminoazines CF3C(NHR)=NN=CClCF3 (6) and the diaminoazines CF3C(NHR)=NN=C(NHR)CF3 (4) by reaction with ammonia or the appropriate primary amino compound; with hydroxylamine the syn-oxime CF3CCl=NNHC(CF3)=NOH (8) (86percent) was formed.The mixed diaminoazines CF3C(NHR)=NN=C(NHR')CF3 (4) have been synthesised from the monoaminoazines 6a-d.A solution of the diaminoazine 4c, heated in ethanol under reflux, gave 3,5-bis(trifluoromethyl)-1H-1,2,4-triazole (1a) (28percent) and its ammonium salt NH4+- (7b) (54percent), while the azines 4g and 4j under the same conditions each afforded 4-phenyl-3,5-bis(trifluoromethyl)-4H-1,2,4-triazole (2c) (ca. 85percent).Thermolysis of the diaminoazines 4c-f and 4h in vacuo over the range 120-150 deg C gave the following results: 4c--->7b (98percent); 4d--->MeNH3+- (7c) (ca. 26percent) + Me4N+- (7d) (ca.13percent) + 4-methyl-3,5-bis(trifluoromethyl)-4H-1,2,4-triazole (2b) (54percent) + 1-methyl-3,5-bis(trifluoromethyl)-1H-1,2,4-triazole (1b) (1.5percent); 4e---> the 4-carbomethoxymethyltriazole (2e) (93percent); 4f---> the 4-carboethoxymethyltriazole (2f) (82percent); 4h--->1a (11percent) + 2b (54percent) + 7c (31percent).Treatment of salt 7b with aqueous hydrochloric acid afforded the triazole 1a (75percent). - Keywords: Unsaturated nitrogen compounds; Synthesis; Bis(trifluoromethyl)triazole; NMR spectroscopy; Mass spectrometry

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