10080-41-8

Basic information

• Product Name: cyclopentylidenehydrazine
• CAS NO: 10080-41-8
• Molecular Formula: C₅H₁₀N₂
• Molecular Weight: 98.1463
• Mol File: 10080-41-8.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 190.9°C at 760 mmHg
• Flash Point: 69.2°C
• Density: 1.14g/cm³
• Vapor Pressure: 0.529mmHg at 25°C
• Refractive Index: 1.568
• CAS DataBase Reference: cyclopentylidenehydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: cyclopentylidenehydrazine(10080-41-8)
• EPA Substance Registry System: cyclopentylidenehydrazine(10080-41-8)

Safety Data

• Hazardous Substances Data: 10080-41-8(Hazardous Substances Data)

Usage

General Description

Cyclopentylidenehydrazine is a chemical compound with the molecular formula C6H12N2. It is a hydrazine derivative that is used in synthetic organic chemistry and is known for its potential applications as a fungicide, insecticide, and plant growth regulator. It has been studied for its potential use in controlling pests in agriculture due to its ability to inhibit the growth of certain pathogens. Cyclopentylidenehydrazine is also being researched for its potential therapeutic applications, particularly as a potential treatment for certain types of cancer. However, its toxicological properties and potential environmental impact are still being investigated.

Upstream product

• 120-92-3 cyclopentanone 

Downstream Products

• 5434-85-5 1-cyclopentene-1-carboxamide 
• 126175-84-6 3-phenyl-1-oxa-2,4-diaza-spiro[4.4]non-2-en4-ylamine 
• 156360-48-4 1-[3-(4-Nitro-phenyl)-1-oxa-2,4-diaza-spiro[4.4]non-2-en-4-yl]-3-phenyl-urea 
• 515835-42-4 (tert-butyl-dimethyl-silanyloxy)-acetic acid 3-benzyloxy-2-tert-butoxycarbonylamino-1-cyclopent-1-enyl-propyl ester 
• 345341-71-1 (R)-2-[(R)-2-(Benzyl-tert-butoxycarbonyl-amino)-3-benzyloxy-prop-(Z)-ylidene]-cyclopentanecarboxylic acid 
• 345341-69-7 Benzyl-{(R)-1-benzyloxymethyl-2-[(R)-2-hydroxymethyl-cyclopent-(Z)-ylidene]-ethyl}-carbamic acid tert-butyl ester 
• 345341-65-3 (1S,2S)-3-Benzyloxy-1-cyclopent-1-enyl-2-dibenzylamino-propan-1-ol 
• 345341-64-2 (S)-3-Benzyloxy-1-cyclopent-1-enyl-2-dibenzylamino-propan-1-one 
• 515835-51-5 {(R)-2-[(R)-2-Benzylamino-3-benzyloxy-prop-(Z)-ylidene]-cyclopentyl}-methanol 
• 515835-47-9 ((1S,2S)-1-Benzyloxymethyl-2-cyclopent-1-enyl-2-hydroxy-ethyl)-carbamic acid tert-butyl ester 
• 515835-41-3 ((1S,2R)-1-Benzyloxymethyl-2-cyclopent-1-enyl-2-hydroxy-ethyl)-carbamic acid tert-butyl ester 
• 515835-39-9 (1-benzyloxymethyl-2-cyclopent-1-enyl-2-oxo-ethyl)-carbamic acid tert-butyl ester 
• 345341-68-6 {(R)-2-[(R)-3-Benzyloxy-2-dibenzylamino-prop-(Z)-ylidene]-cyclopentyl}-methanol 
• 126175-91-5 3-(4-Nitro-phenyl)-1-oxa-2,4-diaza-spiro[4.4]non-2-en-4-ylamine 

Relevant articles and documents

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Amino- and azidocarbonylation of iodoalkenes

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

ALKENE MIMICS

Ac-Phe-Tyr-phosphoSer-Ψ[CH=C]-Pro-Arg-NH2AND Fmoc-bis(pivaloylmethoxy)phosphoSer-Ψ[CH=C]-Pro-2-aminoethyl-(3-indole); and their Phospho-(D)-serine stereoisomers are novel compounds. Ψ refers to a pseudo amide. Such novel compounds advantageousl

Serine-cis-proline and serine-trans-proline isosteres: Stereoselective synthesis of (Z)- and (E)-alkene mimics by Still-Wittig and Ireland-Claisen rearrangements

Two new amide isosteres of Ser-cis-Pro and Ser-trans-Pro dipeptides were designed and stereo-selectively synthesized to be incorporated into potential inhibitors of the phosphorylation-dependent peptidylprolyl isomerase Pin1, an essential regulator of the