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1589-61-3

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1589-61-3 Usage

General Description

Cyclohexanal semicarbazone is a chemical compound formed by the reaction between cyclohexanone and semicarbazide. It is commonly used as a reagent in organic chemistry for the identification and quantification of carbonyl compounds, particularly aldehydes and ketones. Cyclohexanal semicarbazone is a yellow crystalline solid with a melting point of 198-200°C, and it is insoluble in water but soluble in organic solvents such as ethanol and acetone. It is also known for its use as a precursor in the synthesis of various pharmaceuticals, agricultural chemicals, and other organic compounds. Additionally, cyclohexanal semicarbazone has been studied for its potential anti-inflammatory and anti-tumor properties, making it of interest for medical and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 1589-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1589-61:
(6*1)+(5*5)+(4*8)+(3*9)+(2*6)+(1*1)=103
103 % 10 = 3
So 1589-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N3O/c8-7(11)10-9-6-4-2-1-3-5-6/h1-5H2,(H3,8,10,11)

1589-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (cyclohexylideneamino)urea

1.2 Other means of identification

Product number -
Other names 2-cyclohexylidene-hydrazinecarboxamide

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:1589-61-3 SDS

1589-61-3Relevant articles and documents

Reaction of 1,2-polyfluoroacylcyclohexanones with semicarbazides

Pashkevich, K. I.,Sevenard, D. V.,Khomutov, O. G.,Shishkin, O. V.,Solomovich, E. V.

, p. 359 - 363 (1999)

2-Polyfluoroacylcyclohexanones react with semicarbazide and thiosemicarbazide to give 2-(thio)carbamoyl-3-polyfluoroalkyl-3,3a,4,5,6,7-hexahydro-2H-indazoles, one of which was studied by X-ray diffraction.

Investigating the synergism of some hydrazinecarboxamides and iodide ions as corrosion inhibitor formulations for mild steel in hydrochloric Acid: Experimental and computational studies

Adekunle, Abolanle S.,Aniki, Nancy I.,Durodola, Solomon S.,Durosinmi, Lateefa M.,Ebenso, Eno E.,O. Wahab, Olaide,Olasunkanmi, Lukman O.

, (2021/10/01)

Three hydrazinecarboxamides, namely, 2-cyclohexylidenehydrazinecarboxamide (SCYHEX), 2-(pentan-3-ylidene)hydrazinecarboxamide (SP3ONE) and 2-(pentan-2-ylidene)hydrazinecarboxamide (SP2ONE) were tested as inhibitors of acid corrosion of mild steel both without and with addition of iodide ions. The formulated inhibitor solutions showed excellent corrosion inhibition efficiency as they suppressed steel to the tune of 82% without KI additive, and up to 97% with KI additive. The shifts in corrosion potentials recorded from polarization measurements were anodic and ranged from 25 mV to 55 mV (without KI) relative to the uninhibited electrolyte, suggesting that the Schiff bases are mixed-type corrosion inhibitors with prominent effects on anodic dissolution of steel. The inhibitors adsorb at steel/electrolyte interface as reveled by the AC impedance measurements that showed more than 5 times increase in the charge transfer resistance and equivalence decrease in double layer capacitance of the inhibitor-containing solutions compared to the blank. Theoretical density functional theory (DFT) calculations suggested possible covalent interactions between the Schiff bases molecules and Fe with Fe—N and Fe—C bond lengths ranging from 1.87 ? to 1.96 ?. Experimentally derived synergistic parameters for Schiff bases-iodide ions interactions were generally greater than 1 and a strong H—I bond of ca. 2.3 ? length was observed in what appeared to be first time theoretical modelling of inhibitor-iodide ion synergistic interactions. DFT derived reactivity indices of protonated Schiff bases molecules correlated with the observed strengths of corrosion inhibition. Monte Carlo simulations study also confirmed the tendency of the inhibitor molecules to adsorb on mild steel surface and displace corrosive ions from the steel surface.

Basic alumina as an efficient catalyst for preparation of semicarbazones in solvent free conditions

Kiasat, Ali Reza,Kazemi, Foad,Mehrjardi, Mehdi Fallah

, p. 1337 - 1339 (2008/03/13)

An efficient and simple procedure for conversion of different classes of aldehydes and ketones into the corresponding semicarbazones with semicarbazide hydrochloride using basic alumina is studied.

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