Quality Level
assay
95%
form
solid
reaction suitability
reaction type: C-C Bond Formation
impurities
<5% DMF
mp
132 °C (dec.) (lit.)
functional group
amine, chloro
storage temp.
2-8°C
SMILES string
[Cl-].C\[N+](C)=C\Cl
InChI
1S/C3H7ClN.ClH/c1-5(2)3-4;/h3H,1-2H3;1H/q+1;/p-1
InChI key
QQVDYSUDFZZPSU-UHFFFAOYSA-M
Application
用 β-氨基酸通过羧基活化与环化脱水作用来制备 β-内酰胺的试剂。也用于将 α-氨基腈转化为 4-氯咪唑。
用于合成以下物质的试剂或反应物:
用于研究染料敏化太阳能电池中的有机光敏剂
- β-Staudinger 反应中的内酰胺
- 通过NH-吲哚与乙烯基溴的交叉耦合得到的 N-乙烯基取代吲哚
- 多环融合 2-吡啶酮基荧光支架
- 酯前体药物作为抗痘病毒药物
- 用于检测 G-四链体形成的三甲胺菁染料
- 磷脂酰丝氨酸等排体(通过 Hundsdiecker-Barton 碘十二羧基化反应)
- 经由 [2 + 2]-环加成的 2-氮杂环丁酮
用于研究染料敏化太阳能电池中的有机光敏剂
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1A
supp_hazards
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Tetrahedron Letters, 47, 5451-5451 (2006)
J. Chem. Res. (M), 705-705 (2005)
Azhar Abbas et al.
Bioorganic chemistry, 82, 163-177 (2018-10-16)
Benzohydrazide derivatives 1-43 were synthesized via "one-pot" reaction and structural characterization of these synthetic derivatives was carried out by different spectroscopic techniques such as 1H NMR and EI-MS. The synthetic molecules were evaluated for their in vitro urease inhibitory activity.
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 280909-25G | 04061835554874 |
| 280909-5G | 04061833321164 |


