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Cyclohexanone methylhydrazone is an organic compound with the chemical formula C8H15N2O. It is a derivative of cyclohexanone, where a methylhydrazone group (-CH2NHNH2) is attached to the carbonyl group of cyclohexanone. Cyclohexanone, methylhydrazone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as a chiral auxiliary in asymmetric synthesis. Cyclohexanone methylhydrazone is a colorless to pale yellow liquid with a characteristic amine-like odor. It is soluble in common organic solvents and has a melting point of around 40-42°C. The compound is synthesized by reacting cyclohexanone with methylhydrazine in the presence of an acid catalyst. Due to its reactivity and potential applications, cyclohexanone methylhydrazone is an important intermediate in the chemical industry.

1567-83-5

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1567-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567-83-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1567-83:
(6*1)+(5*5)+(4*6)+(3*7)+(2*8)+(1*3)=95
95 % 10 = 5
So 1567-83-5 is a valid CAS Registry Number.

1567-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexylidene-2-methylhydrazine

1.2 Other means of identification

Product number -
Other names Cyclohexanon-N-methyl-hydrazon

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:1567-83-5 SDS

1567-83-5Relevant academic research and scientific papers

Catalytic asymmetric synthesis of 4-nitropyrazolidines: An access to optically active 1,2,3-triamines

Lykke, Lennart,Carlsen, Bj?rn Drei?,Rambo, Raoní Scheibler,J?rgensen, Karl Anker

supporting information, p. 11296 - 11299 (2014/09/17)

The first catalytic enantio- and diastereoselective synthesis of 4-nitropyrazolidines is presented. Asymmetric hydrogen-bonding activation of nitro-olefins facilitated the 1,3-dipolar cycloaddition with hydrazones, affording optically active 4-nitropyrazo

Method for preparing 1,3,4-substituted pyrazol compounds

-

Page/Page column 10, (2011/08/03)

The invention provides an Ethernet bridge or router comprising a network fabric adapted to provide interconnectivity to a plurality of Ethernet ports, each of the Ethernet ports being adapted to receive and/or transmit Ethernet frames, and wherein the Ethernet bridge or router further comprises an encapsulator connected to receive Ethernet Protocol Data Units from the Ethernet ports, wherein the encapsulator is operable to generate a Fabric Protocol Data Unit from a received Ethernet Protocol Data Unit, the Fabric Protocol Data Unit comprising a header portion, and a payload portion which comprises the Ethernet Protocol Data Unit concerned, and wherein the encapsulator is operable to transform Ethernet destination address information from the Ethernet Protocol Data Unit into a routing definition for the network fabric, and to include this routing definition in the header portion of the Fabric Protocol Data Unit. Also provided is a method of data delivery across a network.

Catalytic hydrophosphorylation of alkyl- and acylhydrazones

Matveeva,Podrugina,Kolesnikova,Prisyazhnoi,Karateev,Zefirov

experimental part, p. 418 - 424 (2011/02/17)

N-Boc- and N-acylhydrazino phosphonates were obtained for the first time by hydrophos- phorylation of the appropriate hydrazones of aliphatic and aromatic aldehydes and heterocyclic and aliphatic ketones in the presence of [tetra(tert-butyl)phthalocyanine

Role of Spacer and Address Components in Peptidomimetic δ Opioid Receptor Antagonists Related to Naltrindole

Portoghese, P. S.,Nagase, H.,MaloneyHuss, K. E.,Lin, C.-E.,Takemori, A. E.

, p. 1715 - 1720 (2007/10/02)

A series of heterocyclic analogues 2-5 related to naltrindole (1) (NTI) and 6-arylnaltrexone derivatives 6-8 were synthesized in order to determine the role of the spacer and the address moieties in conferring δ opioid receptor antagonist activity.The ben

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