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50707-40-9

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50707-40-9 Usage

General Description

1-ETHYL-3-P-TOLYLTRIAZENE is a compound consisting of a triazene group with an ethyl and para-tolyl substituents. It is primarily used as a reagent in chemical research and is not commonly found in consumer products or industrial applications. The compound is not well-studied in terms of its specific properties and potential uses, but research suggests it may have potential applications in the field of organic synthesis and pharmaceutical development. Its chemical structure and reactivity make it a potentially valuable tool for creating new molecules with specific properties. However, further research is needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 50707-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,0 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50707-40:
(7*5)+(6*0)+(5*7)+(4*0)+(3*7)+(2*4)+(1*0)=99
99 % 10 = 9
So 50707-40-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N3/c1-3-10-12-11-9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3,(H,10,11)

50707-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ETHYL-3-P-TOLYLTRIAZENE

1.2 Other means of identification

Product number -
Other names Ethyltolyltriazene

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:50707-40-9 SDS

50707-40-9Relevant articles and documents

Novel one-pot synthesis of thiophenols from related triazenes under mild conditions

Khazaei, Ardeshir,Kazem-Rostami, Masoud,Moosavi-Zare, Ahmadreza,Bayat, Mohammad,Saednia, Shahnaz

experimental part, p. 1893 - 1896 (2012/09/22)

In this work, at first, triazenes were synthesized from primary aryl amines. Afterwards, triazenes were converted into the corresponding thiophenols in one-pot using sodium sulfide in acidic media, by in situ generation of diazonium counterion beside hydrogen sulfide as anionic sulfur nucleophile at room temperature. The procedure can be a convenient shortcut for the preparation of thiophenols from primary aryl amines. Georg Thieme Verlag Stuttgart · New York.

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