Cyclohexanecarboxamide
- Name Cyclohexanecarboxamide
- CAS 1122-56-1
- Purity 99%
Product Details
Manufacturer supply high quality Cyclohexanecarboxamide 1122-56-1 with ISO standards
- Molecular Formula: C7H13NO
- Molecular Weight: 127.186
- Appearance/Colour: White amorphous powder
- Vapor Pressure: 0.00386mmHg at 25°C
- Melting Point: 186-188 °C(lit.)
- Refractive Index: 1.484
- Boiling Point: 280.1 °C at 760 mmHg
- PKA: 16.76±0.20(Predicted)
- Flash Point: 123.2 °C
- PSA： 43.09000
- Density: 1.018 g/cm3
- LogP: 1.75230
Cyclohexanecarboxamide(Cas 1122-56-1) Usage
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Synthesis Reference(s) |
The Journal of Organic Chemistry, 44, p. 4727, 1979 DOI: 10.1021/jo00393a063 |
|
General Description |
The enthalpy of dilution of cyclohexanecarboxamide in N,N-dimethylformamide was studied to evaluate the enthalpic interaction coefficient. |
|
Safety Profile |
A skin irritant. When heated to decomposition it emits toxic fumes of NOx. |
InChI:InChI=1/C7H13NO/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2,(H2,8,9)
1122-56-1 Relevant articles
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Gipson,R.M. et al.
, p. 1425 - 1426 (1963)
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Half-Sandwich Iridium Complexes for the One-Pot Synthesis of Amides: Preparation, Structure, and Diverse Catalytic Activity
Fan, Xiao-Nan,Deng, Wei,Liu, Zhen-Jiang,Yao, Zi-Jian
, p. 16582 - 16590 (2020)
Several types of air-stable N,O-coordina...
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Kornblum,N.,Singaram,S.
, p. 4727 - 4729 (1979)
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A general and practical oxidation of alcohols to primary amides under metal-free conditions
Wu, Xiao-Feng,Sharif, Muhammad,Feng, Jian-Bo,Neumann, Helfried,Pews-Davtyan, Anahit,Langer, Peter,Beller, Matthias
, p. 1956 - 1961 (2013)
A general procedure for oxidation of bot...
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Raber et al.
, p. 7671 (1977)
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Chemoselective hydrogenation of heteroarenes and arenes by Pd-Ru-PVP under mild conditions
Abe, Naoya,Chaudhari, Chandan,Ikeda, Yasuyuki,Kitagawa, Hiroshi,Kusuda, Kohei,Matsumura, Syo,Nagaoka, Katsutoshi,Nishida, Yoshihide,Sato, Katsutoshi,Terada, Kenji,Toriyama, Takaaki,Yamamoto, Tomokazu
, p. 44191 - 44195 (2020)
Monometallic (Pd, Ru or Rh) and bimetall...
RhI-catalyzed hydration of organonitriles under ambient conditions
Goto, Akihiro,Endo, Kohei,Saito, Susumu
, p. 3607 - 3609 (2008)
(Chemical Presented) New scoop on scope ...
Phosphinous Acid-Assisted Hydration of Nitriles: Understanding the Controversial Reactivity of Osmium and Ruthenium Catalysts
González-Fernández, Rebeca,Crochet, Pascale,Cadierno, Victorio,Menéndez, M. Isabel,López, Ramón
, p. 15210 - 15221 (2017)
The synthesis and catalytic behavior of ...
An environmentally benign electrochemical process for the reduction of carboxylic acid hydrazides to amides
Mentel, Matthias,Beier, Matthias J.,Breinbauer, Rolf
, p. 1463 - 1468 (2009)
The transformation of acid hydrazides to...
Activation of nitriles by silver(I) N-heterocyclic carbenes: An efficient on-water synthesis of primary amides
Thirukovela, Narasimha Swamy,Balaboina, Ramesh,Kankala, Shravankumar,Vadde, Ravindhar,Vasam, Chandra Sekhar
, p. 2637 - 2641 (2019)
A first example of silver(I) N-heterocyc...
Investigation of binap-based hydroxyphosphine arene-ruthenium(II) complexes as catalysts for nitrile hydration
Toms-Mendivil, Eder,Menndez-Rodrguez, Luca,Francos, Javier,Crochet, Pascale,Cadierno, Victorio
, p. 63466 - 63474 (2014)
The binap-based hydroxyphosphine-(η6-are...
Amides from Nitriles using Basic Hydrogen Peroxide under Phase-Transfer Catalyzed Conditions
Cacchi, S.,Misiti, D.,Torre, F. La
, p. 243 - 244 (1980)
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Ceria supported Ru0-Ruδ+ clusters as efficient catalyst for arenes hydrogenation
Cao, Yanwei,Zheng, Huan,Zhu, Gangli,Wu, Haihong,He, Lin
supporting information, p. 770 - 774 (2020/08/24)
Selective hydrogenation of aromatic amin...
PRODUCTION METHOD OF CYCLIC COMPOUND
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Paragraph 0057; 0060; 0062; 0065, (2021/05/05)
PROBLEM TO BE SOLVED: To provide an indu...
Half-Sandwich Iridium Complexes Based on β-Ketoamino Ligands: Preparation, Structure, and Catalytic Activity in Amide Synthesis
Wang, Yang,Guo, Wen,Guan, Ai-Lin,Liu, Shuang,Yao, Zi-Jian
, p. 11514 - 11520 (2021/07/31)
A series of β-ketoamino-based N,O-chelat...
A Molecular Iron-Based System for Divergent Bond Activation: Controlling the Reactivity of Aldehydes
Chatterjee, Basujit,Jena, Soumyashree,Chugh, Vishal,Weyhermüller, Thomas,Werlé, Christophe
, p. 7176 - 7185 (2021/06/30)
The direct synthesis of amides and nitri...
1122-56-1 Process route
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55-21-0,27208-38-4
benzamide
-
-
3309-27-1
N,N-dicyclohexylmethylamine
-
-
1122-56-1
cyclohexylcarboxamide
-
-
3218-02-8
cyclohexylmethylamine
-
-
100-49-2
cyclohexylmethyl alcohol
| Conditions | Yield |
|---|---|
|
With
hydrogen; lithium hydroxide;
In
1,2-dimethoxyethane;
at 160 ℃;
for 16h;
under 75007.5 Torr;
|
-
-
64-17-5
ethanol
-
-
7732-18-5
water
-
-
55-21-0,27208-38-4
benzamide
-
-
1122-56-1
cyclohexylcarboxamide
-
-
100-51-6,185532-71-2
benzyl alcohol
| Conditions | Yield |
|---|---|
|
|
1122-56-1 Upstream products
-
4630-82-4
methyl cyclohexylcarboxylate
-
94052-40-1
methyl cyclohexanecarboximidate hydrochloride
-
766-05-2
cyclohexane carbonitrile
-
38941-47-8
cyclohexanecarbohydrazide
1122-56-1 Downstream products
-
100723-03-3
N -cyclohexyl-N -formyl-N' -phenyl-urea
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5817-68-5
cyclohexyl-carbamic acid methyl ester
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104462-82-0
2-cyclohexylbenzoxazole
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766-05-2
cyclohexane carbonitrile
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