C11006
碳酰肼
98%
别名:
1,3-二氨基脲, N,N′-二氨基脲, 碳酰二肼, 碳酰肼
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关于此项目
线性分子式:
CO(NHNH2)2
化学文摘社编号:
分子量:
90.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-837-2
Beilstein/REAXYS Number:
1747069
MDL number:
Assay:
98%
Form:
crystals
产品名称
碳酰肼, 98%
InChI
1S/CH6N4O/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)
InChI key
XEVRDFDBXJMZFG-UHFFFAOYSA-N
SMILES string
NNC(=O)NN
assay
98%
form
crystals
mp
150-153 °C (lit.)
Quality Level
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Application
碳酰肼用于：
- 作为除氧剂。
- 通过缩合反应，与各种醛和配体合成多齿席夫碱配体。
- 通过环缩合反应合成含三氟甲基的（E）-N′--亚芳基-1-H-吡唑-1-碳酰肼，具有抗氧化剂和抗菌特性。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1
supp_hazards
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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
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
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)
Ameen Ali Abu-Hashem et al.
Acta pharmaceutica (Zagreb, Croatia), 60(3), 311-323 (2010-12-08)
2-Amino-5-acetyl-4-methyl-thiophene-3-carboxylic acid ethyl ester (1) and 5-acetyl-2-amino-4-methylthiophene-3-carbohydrazide (2) were synthesized and used as starting materials for the synthesis of new series of 1-(5-amino-4-(3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3a), 1-(5-amino-4-(4-chloro-3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3b), 1-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl)pyrazolidine-3,5-dione (4), (Z)-N'-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl) formohydrazonic acid (5a), (Z)-ethyl-N'-4-methyl-2-amino-5-acetylthiophene-3-carbonylformo hydrazonate (5b), 6-acetyl-3-amino-2,5-dimethylthieno[2,3-d]pyrimidin-4(3H)-one (8), 5-methyl-3-amino-2-mercapto-6-acetylthieno
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