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3,4-dimethyl-3-penten-2-one tosylhydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82323-80-6

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82323-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82323-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,2 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82323-80:
(7*8)+(6*2)+(5*3)+(4*2)+(3*3)+(2*8)+(1*0)=116
116 % 10 = 6
So 82323-80-6 is a valid CAS Registry Number.

82323-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dimethyl-3-penten-2-one tosylhydrazone

1.2 Other means of identification

Product number -
Other names Methylmesityloxid-tosylhydrazon

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:82323-80-6 SDS

82323-80-6Downstream Products

82323-80-6Relevant academic research and scientific papers

Thermolysis of Vinyldiazomethanes as a Method for the Generation of Vinylcarbenes and a Comparison with Cyclopropene Photochemistry

Pincock, James A.,Mathur, Naresh C.

, p. 3699 - 3706 (2007/10/02)

The pyrolysis of the vinyldiazomethanes 6 (X = H), 8, 9, and 10 gives mixtures of 3H-pyrazoles and cyclopropenes.The kinetics and product distribution for each case lead to a determination of the rate of vinylcarbene formation and, therefore, a direct determination of the relative carbene stabilities.The conclusion is that carbene 14 is more stable than 15.These results are then used as a basis for a discussion of the carbenes generated from the singlet photochemistry of unsymmetrical cyclopropenes, 11.

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