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C11006

Sigma-Aldrich

Carbohydrazide

98%

Sinônimo(s):

1,3-Diaminourea, Carbodihydrazide, Carbonohydrazide, N,N′-Diaminourea

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About This Item

Fórmula linear:
CO(NHNH2)2
Número CAS:
497-18-7
Peso molecular:
90.08
Beilstein:
1747069
Número CE:
207-837-2
Número MDL:
MFCD00007591
Código UNSPSC:
12352100
ID de substância PubChem:
24892343
NACRES:
NA.22

Ensaio

98%

forma

crystals

pf

150-153 °C (lit.)

cadeia de caracteres SMILES

NNC(=O)NN

InChI

1S/CH6N4O/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)

chave InChI

XEVRDFDBXJMZFG-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

Carbohydrazide can be used:
  • As an oxygen scavenger.
  • In the synthesis of polydentate Schiff base ligands with various aldehydes and ligands by condensation.
  • In the synthesis of trifluoromethyl-containing (E)-N′-arylidene-1H-pyrazole-1-carbohydrazides by cyclocondensation reaction which shows antioxidant and antimicrobial properties.

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H302,H315,H317,H411

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1

Perigos de suplementos

EUH044

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Alessandro K Jordão et al.
Bioorganic & medicinal chemistry, 19(18), 5605-5611 (2011-08-16)
Tuberculosis treatment remains a challenge that requires new antitubercular agents due to the emergence of multidrug-resistant Mycobacterium strains. This paper describes the synthesis, the antitubercular activity and the theoretical analysis of N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides (8a-b, 8e-f, 8i-j and 8n-o) and new analogues
Paolo Mombelli et al.
ChemMedChem, 7(1), 151-158 (2011-11-19)
A series of inhibitors of plant enzymes of the non-mevalonate pathway from herbicide research efforts at BASF were screened for antimalarial activity in a cell-based assay. A 1,3-diiminoisoindoline carbohydrazide was found to inhibit the growth of Plasmodium falciparum with an
New trifluoromethyl-containing (E)-N?-arylidene-[3-alkyl (aryl/heteroaryl)-4, 5-dihydro-1H-pyrazol-1-yl] carbohydrazides: Synthesis, crystal structure and antimicrobial/antioxidant activity.
Bonacorso HG, et al.
Journal of Fluorine Chemistry, 135(10), 303-314 (2012)
Huisheng Huang et al.
Journal of hazardous materials, 179(1-3), 21-27 (2010-04-07)
The molecular geometry, electronic structure, infrared spectra and thermochemical properties of cobalt and nickel tris(carbohydrazide) perchlorates (CoCP and NiCP) as well as copper bis(carbohydrazide) perchlorate (CuCP) were investigated using the Heyd-Scuseria-Ernzerhof (HSE) screened hybrid density functional. The results show that
Experimental investigation and optimization of carbohydrazide application using different alkalization agents on boilers All-Volatile treatment.
Vasile-Pafili SMV and Bartzis JG
Applied Thermal Engineering, 30(10), 1269-1275 (2010)
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