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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
NH2CONHNH2 · HCl
CAS 번호:
Molecular Weight:
111.53
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-247-0
Beilstein/REAXYS Number:
3593642
MDL number:
Assay:
≥99%
InChI key
XHQYBDSXTDXSHY-UHFFFAOYSA-N
InChI
1S/CH5N3O.ClH/c2-1(5)4-3;/h3H2,(H3,2,4,5);1H
SMILES string
Cl.NNC(N)=O
assay
≥99%
mp
175-177 °C (dec.) (lit.)
Quality Level
유사한 제품을 찾으십니까? 방문 제품 비교 안내
Application
Derivatization reagent for aldehydes and ketones which produces crystalline compounds with characteristic melting points.
Semicarbazide hydrochloride is a general reagent used to synthesize semicarbazones from aldehydes and ketones. It can be used to build a variety of heterocyclic compounds, some of which are potent antimicrobial and antiviral agents. It can also be used to prepare corrosion inhibitors.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 Oral
target_organs
Bone
저장 등급
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Synthesis of some new azole, azepine, pyridine, and pyrimidine derivatives using 6?hydroxy?4H?4?oxo [1]?benzopyran?3?carboxaldehyde as a versatile starting material.
Abdel?Rahman A H, et al.
Heteroatom Chem., 16(1), 20-27 (2005)
Synthesis and antimalarial activity of semicarbazone and thiosemicarbazone derivatives.
de Oliveira R B, et al.
European Journal of Medicinal Chemistry, 43(9), 1983-1988 (2008)
Design, synthesis, and biological evaluation of antiviral agents targeting flavivirus envelope proteins.
Li Z, et al.
Journal of Medicinal Chemistry, 51(15), 4660-4671 (2008)
Experimental and theoretical evaluation of semicarbazones and thiosemicarbazones as organic corrosion inhibitors.
Goulart C M, et al.
Corrosion Science, 67, 281-291 (2013)
Semicarbazide.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
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