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Cyclohexanone, 4-(1,1-dimethylethyl)-, hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62082-37-5

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62082-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62082-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,8 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62082-37:
(7*6)+(6*2)+(5*0)+(4*8)+(3*2)+(2*3)+(1*7)=105
105 % 10 = 5
So 62082-37-5 is a valid CAS Registry Number.

62082-37-5SDS

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 (4-tert-butylcyclohexylidene)hydrazine

1.2 Other means of identification

Product number -
Other names Cyclohexanone,4-(1,1-dimethylethyl)-,hydrazone

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:62082-37-5 SDS

62082-37-5Upstream product

62082-37-5Relevant academic research and scientific papers

Amino- and azidocarbonylation of iodoalkenes

Mikle, Gábor,Skoda-F?ldes, Rita,Kollár, László

, (2021/10/14)

Iodoalkenes, available from ketones via their hydrazones, underwent palladium-catalysed azidocarbonylation. Depending on the structure of the acyl azides, consecutive hydrolysis toward corresponding primary amides was observed. ‘Direct’ aminocarbonylation

STUDIES ON THE OXIDATION OF HYDRAZONES WITH IODINE AND WITH PHENYLSELENENYL BROMIDE IN THE PRESENCE OF STRONG ORGANIC BASES; AN IMPROVED PROCEDURE FOR THE SYNTHESIS OF VINYL IODIDES AND PHENYL-VINYL SELENIDES

Barton, Derek H. R.,Bashiardes, George,Fourrey, Jan-Louis

, p. 147 - 162 (2007/10/02)

The oxidation of hydrazones by iodine in the presence of strong organic bases (guanidines) has been studied.Improved yields of vinyl iodides can be obtained by inverse addition using dry solvents and with a final heating period where appropriate.The reaction has been extended to various dihydrazones with interesting results.In complementary studies hydrazones have been oxidized by phenylselenyl bromide in the presence of strong organic bases to give the corresponding phenyl vinyl selenides in good yield.

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