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Merck
모든 사진(2)

Key Documents

O9328

Sigma-Aldrich

Oxamide

98%

동의어(들):

Oxalic acid diamide

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About This Item

Linear Formula:
NH2COCONH2
CAS Number:
Molecular Weight:
88.07
Beilstein:
1743262
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

형태

powder

mp

>300 °C (lit.)

SMILES string

NC(=O)C(N)=O

InChI

1S/C2H4N2O2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)

InChI key

YIKSCQDJHCMVMK-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Oxamide can be used:
  • As a precursor for the synthesis of ligands such as bis(benzimidazole) and Schiff base ligands formed by condensation with furfural.
  • Carbon nitride (g-C3N4) nanotubes by self-assembly polymerization with urea.
  • As a bridging ligand for the synthesis of binuclear IrIII complex [Ir22-oxamidato-N,N′,O,O′)(ptpy)4], ptpy = 2-(p-tolyl)pyridinato.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

T L Nguyen et al.
Journal of the American Chemical Society, 123(44), 11057-11064 (2001-11-01)
Ureas characteristically form one-dimensional hydrogen-bonded alpha-networks with a repeat distance of about 4.60 A. Oxamides form similar alpha-networks with a longer 5.05 A repeat distance. The urea of glycine and the oxamide of glycine were each cocrystallized with a series
Advancing the n?π* electron transition of carbon nitride nanotubes for H2 photosynthesis
Zhang G, et al.
Journal of Material Chemistry A, 5(25), 12723-12728 (2017)
Bis (benzimidazole) as supramolecular building block in manganese (IV) chemistry
Samol'ova E, et al.
Journal of Molecular Structure, 1176, 366-375 (2019)
E Armelin et al.
The Journal of organic chemistry, 66(24), 8076-8085 (2001-11-28)
The conformational properties of the oxalamide group and crystal structure of several polyoxalamides have been investigated by computational methods. First, a detailed quantum mechanical study of the conformational preferences of N,N'-dimethyloxalamide is reported. Results, which were obtained at the MP2/6-31G(d)
Synthesis, characterization, and biological and anticancer studies of mixed ligand complexes with Schiff base and 2, 2?-bipyridine
Omar MM, et al.
Applied Organometallic Chemistry, 31(10), e3724-e3724 (2017)

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