Merck
CN

120685

Sigma-Aldrich

N-环己基甲酰胺

99%

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线性分子式:
HCONHC6H11
CAS号:
分子量:
127.18
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

形式

solid

bp

113 °C/700 mmHg (lit.)

mp

36-41 °C (lit.)

SMILES string

O=CNC1CCCCC1

InChI

1S/C7H13NO/c9-6-8-7-4-2-1-3-5-7/h6-7H,1-5H2,(H,8,9)

InChI key

SWGXDLRCJNEEGZ-UHFFFAOYSA-N

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此商品
196746481907183601
N-Cyclohexylformamide 99%

Sigma-Aldrich

120685

N-环己基甲酰胺

2,3,4,5,6-Pentafluorobenzyl alcohol 98%

Sigma-Aldrich

196746

2,3,4,5,6-五氟苯甲醇

Nicotinamide Precursor of the coenzymes NAD+ and NADP+.

Millipore

481907

Nicotinamide

2,5-Dichlorobenzyl alcohol 99%

Sigma-Aldrich

183601

2,5-二氯苯甲醇

form

solid

form

solid

form

solid

form

powder

bp

113 °C/700 mmHg (lit.)

bp

114-115 °C/60 mmHg (lit.)

bp

-

bp

-

mp

36-41 °C (lit.)

mp

37-38 °C (lit.)

mp

-

mp

79-80 °C (lit.)

Gene Information

human ... ADH1A(124), ADH1B(125), ADH1C(126), ADH4(127), ADH7(131), EPHX2(2053)
mouse ... Ephx2(13850)

Gene Information

-

Gene Information

-

Gene Information

-

一般描述

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 .

应用

N-Cyclohexylformamide was used in the synthesis of 2-methylidene-1,3-selenazolidine derivatives.

象形图

CorrosionExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

235.4 °F - closed cup

闪点(°C)

> 113 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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N-Methylformamide 99%

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N-甲基甲酰胺

Sodium pyrophosphate tetrabasic ≥95%

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焦磷酸钠 四元

N,N-Dimethylformamide anhydrous, 99.8%

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N,N-二甲基甲酰胺

H Deng et al.
Biochemistry, 37(40), 14267-14278 (1998-10-07)
The binding of N-cyclohexylformamide (CXF) to the complex of horse liver alcohol dehydrogenase with NADH mimics that of the Michaelis complex for aldehyde reduction catalyzed by the enzyme. The Raman spectra of bound CXF and its 13C- and 15N-substituted derivatives
M Goda et al.
The Journal of biological chemistry, 276(26), 23480-23485 (2001-04-18)
Isonitrile containing an N triple bond C triple bond was degraded by microorganism sp. N19-2, which was isolated from soil through a 2-month acclimatization culture in the presence of this compound. The isonitrile-degrading microorganism was identified as Pseudomonas putida. The
Selenium-containing heterocycles from isoselenocyanates: synthesis of 2-methylidene-1, 3-selenazolidine derivatives.
Sommen GL, et al.
Tetrahedron, 62(14), 3344-3354 (2006)
S Ramaswamy et al.
Biochemistry, 36(12), 3522-3527 (1997-03-25)
Amides are analogs of aldehydes and potent inhibitors of liver alcohol dehydrogenases. They can be used for structural studies and for inhibiting the metabolism of alcohols that form toxic products. We studied N-alkyl amides that bind to the enzyme-NADH complex
Uncompetitive inhibitors of alcohol dehydrogenases.
B V Plapp et al.
Advances in experimental medicine and biology, 463, 295-303 (1999-06-03)

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