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6333-84-2

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6333-84-2 Usage

General Description

(E)-bis(3,4,5-trimethoxyphenyl)diazene, also known as bis(3,4,5-trimethoxyphenyl) diimine, is a chemical compound with the molecular formula C20H24N2O6. It is a diazene derivative, which is a type of organic compound containing a pair of double-bonded nitrogen atoms. (E)-bis(3,4,5-trimethoxyphenyl)diazene is characterized by its yellow crystalline form and is typically used in organic synthesis and as a reagent in chemical reactions. However, it is important to handle this compound with caution as it is potentially hazardous to health and the environment. Its specific uses and properties would depend on the particular application and context in which it is being used.

Check Digit Verification of cas no

The CAS Registry Mumber 6333-84-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6333-84:
(6*6)+(5*3)+(4*3)+(3*3)+(2*8)+(1*4)=92
92 % 10 = 2
So 6333-84-2 is a valid CAS Registry Number.

6333-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(3,4,5-trimethoxyphenyl)diazene

1.2 Other means of identification

Product number -
Other names bis-(3,4,5-trimethoxy-phenyl)-diazene

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:6333-84-2 SDS

6333-84-2Upstream product

6333-84-2Downstream Products

6333-84-2Relevant articles and documents

In-depth examination of the pterolactams behaviour in Lewis/Br?nsted acid catalysis environment: Total isolation of the reaction products

Dumitriu, Gina-Mirabela,B?cu, Elena,Rigo, Beno?t,Moncol, Ján,Da?ch, Adam,Ghinet, Alina

, (2021/01/20)

To gain some insights on the amidoalkylation process, we were interested in studying the product distribution when pterolactam was exposed to acids. The reactivity of pterolactam and its N-aryl derivatives towards TMSOTf or TfOH has been carefully examine

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