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Cyclohexanecarboxaldehyde - 97%, high purity , CAS No.2043-61-0

    Grade & Purity:
  • ≥97%
In stock
Item Number
C109681
Grouped product items
SKU Size
Availability
Price Qty
C109681-5ml
5ml
2
$14.90
C109681-25ml
25ml
2
$57.90
C109681-100ml
100ml
1
$167.90
C109681-500ml
500ml
1
$752.90

Basic Description

Synonyms cyclohexylcarbaldehyde | Cyclohexanecarboxaldehyde; | CHEBI:197359 | Cyclohexancarboxaldehyde | cyclohexane carbaldehyde | cyclohexane carboaldehyde | A814556 | Cyclohexanealdehyde | cyclohexane-aldehyde | cyclohexancarbaldehyd | cyclohexyl carboxaldehyde
Specifications & Purity ≥97%
Storage Temp Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Employed in an aldol reaction with ethyl diazoacetate catalyzed by basic, nanoparticulate magnesium oxide leading to α-diazo-β-hydroxyesters

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organic oxides
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Organic oxides
Alternative Parents Hydrocarbon derivatives  Aldehydes  
Molecular Framework Aliphatic homomonocyclic compounds
Substituents Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aliphatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as organic oxides. These are organic compounds containing an oxide group.
External Descriptors Not available

Names and Identifiers

IUPAC Name cyclohexanecarbaldehyde
INCHI InChI=1S/C7H12O/c8-6-7-4-2-1-3-5-7/h6-7H,1-5H2
InChIKey KVFDZFBHBWTVID-UHFFFAOYSA-N
Smiles C1CCC(CC1)C=O
Isomeric SMILES C1CCC(CC1)C=O
WGK Germany 3
UN Number 1989
Molecular Weight 112.17
Beilstein 878306
Reaxy-Rn 878306
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=878306&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot Number Certificate Type Date Item
L2215102 Certificate of Analysis Apr 18, 2025 C109681
A2517148 Certificate of Analysis Jan 21, 2025 C109681
A2517169 Certificate of Analysis Jan 21, 2025 C109681
L2215093 Certificate of Analysis Sep 18, 2024 C109681
L2215122 Certificate of Analysis Sep 18, 2024 C109681
L2215177 Certificate of Analysis Sep 18, 2024 C109681
A2207141 Certificate of Analysis Oct 09, 2023 C109681
A2207144 Certificate of Analysis Oct 09, 2023 C109681
A2207026 Certificate of Analysis Oct 09, 2023 C109681
A2207140 Certificate of Analysis Oct 09, 2023 C109681
G2423076 Certificate of Analysis Nov 28, 2022 C109681
D2014105 Certificate of Analysis Feb 19, 2022 C109681

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Chemical and Physical Properties

Solubility Soluble in chloroform, ether, alcohol. Slightly soluble in water.
Sensitivity Light sensitive;Air sensitive;light sensitive
Refractive Index 1.449-1.452
Flash Point(°F) 105.8 °F
Flash Point(°C) 40℃
Boil Point(°C) 159°C
Melt Point(°C) 34-35℃
Molecular Weight 112.170 g/mol
XLogP3 1.800
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 1
Exact Mass 112.089 Da
Monoisotopic Mass 112.089 Da
Topological Polar Surface Area 17.100 Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 72.500
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Shenghui Zhou, Fanglin Dai, Zhouyang Xiang, Tao Song, Detao Liu, Fachuang Lu, Haisong Qi.  (2019)  Zirconium–lignosulfonate polyphenolic polymer for highly efficient hydrogen transfer of biomass-derived oxygenates under mild conditions.  APPLIED CATALYSIS B-ENVIRONMENTAL,  248  (31). 
2. Yilin Wei, Zhiwei Sun, Qingqing Li, Dan Wu, Jianshe Wang, Yuexing Zhang, Chunbao Charles Xu, Renfeng Nie.  (2024)  Efficient reductive amination of furfural to furfurylamine promoted synergistically by surface Co0 and oxygen-vacant CoOx.  FUEL,  369  (131703). 

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