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N-Cyclohexylformamide - >98.0%(GC), high purity , CAS No.766-93-8

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N-Cyclohexylformamide - >98.0%(GC), high purity , CAS No.766-93-8

COA

Grade & Purity:

≥98%(GC)

Cas Number: 766-93-8
Molecular Weight: 127.19
Beilstein Registry Number: 12(2)11
MDL number: MFCD00003828
PubChem CID: 13017
PubChem SID: 488181770

In stock

Item Number

N159269

Grouped product items
SKU	Size	Availability	Price
N159269-5g	5g	10	$16.90
N159269-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$61.90
N159269-100g	100g	1	$222.90

View related series

amide (313) Non heterocyclic block (8163)

Basic Description

Synonyms	FT-0632914 \| Cyclohexylformamide \| Formamidocyclohexane \| N-Cyclohexylformamide, 99% \| AE-646/31212051 \| DTXSID40227416 \| DB03559 \| CS-0099360 \| N-CYCLOHEXYL FORMAMIDE \| N-Cyclohexylformamid \| UNII-X2CFE4SDT6 \| AI3-16743 \| D89406 \| FORMAMIDE, N-CYCLOHEXYL
Specifications & Purity	≥98%(GC)
Shipped In	Normal
Product Description	N-Cyclohexylformamide binds to the complex of horse liver alcohol dehydrogenase with NADH and is similar to the Michaelis complex for aldehyde reduction catalyzed by the enzyme.It is formed during hydration of cyclohexyl isocyanide catalyzed by a novel enzyme isonitrile hydratase from Pseudomonas putida N19-2. N-Cyclohexylformamide was used in the synthesis of 2-methylidene-1,3-selenazolidine derivatives.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Level5 Carboxylic acid amides
        Level6 Secondary carboxylic acid amides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Carboxylic acid derivatives
Intermediate Tree Nodes	Carboxylic acid amides
Direct Parent	Secondary carboxylic acid amides
Alternative Parents	Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic homomonocyclic compounds
Substituents	Secondary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as secondary carboxylic acid amides. These are compounds containing a secondary carboxylic acid amide functional group, with the general structure RC(=O)N(R')H (R,R'=alkyl, aryl).
External Descriptors	a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

ADH1A Tclin Alcohol dehydrogenase alpha chain (33 Activities)

Discover Target: ADH1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADH7 Tchem Alcohol dehydrogenase class IV (23 Activities)

Discover Target: ADH7

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADH1B Tclin Alcohol dehydrogenase beta chain (24 Activities)

Discover Target: ADH1B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADH1C Tclin Alcohol dehydrogenase gamma chain (23 Activities)

Discover Target: ADH1C

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADH4 Tbio Alcohol dehydrogenase class II (23 Activities)

Discover Target: ADH4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488181770
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488181770
IUPAC Name	N-cyclohexylformamide
INCHI	InChI=1S/C7H13NO/c9-6-8-7-4-2-1-3-5-7/h6-7H,1-5H2,(H,8,9)
InChIKey	SWGXDLRCJNEEGZ-UHFFFAOYSA-N
Smiles	C1CCC(CC1)NC=O
Isomeric SMILES	C1CCC(CC1)NC=O
WGK Germany	2
RTECS	LQ1825000
Molecular Weight	127.19
Beilstein	12(2)11
Reaxy-Rn	2040181
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2040181&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.

8 results found

Lot Number	Certificate Type	Date	Item
H1725014	Certificate of Analysis	Mar 04, 2025	N159269
D2306592	Certificate of Analysis	Mar 15, 2023	N159269
D2306593	Certificate of Analysis	Mar 15, 2023	N159269
D2306683	Certificate of Analysis	Mar 15, 2023	N159269
D2306729	Certificate of Analysis	Mar 15, 2023	N159269
D2306602	Certificate of Analysis	Mar 15, 2023	N159269
D2306608	Certificate of Analysis	Mar 15, 2023	N159269
C2209207	Certificate of Analysis	May 21, 2022	N159269

Chemical and Physical Properties

Solubility	Soluble in Methanol
Flash Point(°F)	>235.4 °F
Flash Point(°C)	>113 °C
Boil Point(°C)	151 °C/17 mmHg
Melt Point(°C)	30 °C
Molecular Weight	127.180 g/mol
XLogP3	1.400
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	127.1 Da
Monoisotopic Mass	127.1 Da
Topological Polar Surface Area	29.100 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	86.900
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

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