所有图片(1)
About This Item
线性分子式:
O2NC6H3(SCN)NH2
CAS号:
分子量:
195.20
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
95%
表单
solid
mp
113 °C (lit.)
SMILES字符串
Nc1ccc(SC#N)cc1[N+]([O-])=O
InChI
1S/C7H5N3O2S/c8-4-13-5-1-2-6(9)7(3-5)10(11)12/h1-3H,9H2
InChI key
QUWHIBBGKKRYFW-UHFFFAOYSA-N
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Synthesis of 2-Amino-5 (6)-(4-aminophenyl) benzimidazole Derivatives: II. Reaction of 2-Nitro-4-thiocyanatoaniline with 4-Nitrochlorobenzene.
Pilyugin VS, et al.
Russ. J. Org. Chem., 39(7), 979-984 (2003)
Reaction of 2-Nitro-4-thiocyanatoaniline with 4-Nitrochlorobenzene.
Pilyugin VS, et al.
Russ. J. Gen. Chem., 72(9), 1439-1443 (2002)
Andreas Schmidt et al.
Organic & biomolecular chemistry, 1(23), 4342-4350 (2003-12-20)
2,3-Diaminophenol 4, 3,4-diaminophenol 5, 4-methoxy-1,2-diaminobenzene 6, 3,4-diaminobenzenethiol 7, 2,3-diaminobenzoic acid 8, and 3,4-diaminobenzoic acid 9 were reacted with 2,4-pentanedione to yield the corresponding benzo[b][1,4]diazepinium salts, respectively. The hydroxy-benzo[b][1,4]diazepinium salts 17 and 18 do not form mesomeric betaines (MB) on deprotonation.
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