857661
4-氨基联苯胺 二盐酸盐
98%
别名:
p-氨基苯甲酰胺二盐酸盐
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关于此项目
线性分子式:
H2NC6H4C(=NH)NH2·2HCl
化学文摘社编号:
分子量:
208.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-692-2
Beilstein/REAXYS Number:
3692927
MDL number:
Assay:
98%
Form:
crystals
Quality Level
assay
98%
form
crystals
mp
>300 °C (lit.)
functional group
amine
storage temp.
2-8°C
SMILES string
Cl[H].Cl[H].NC(=N)c1ccc(N)cc1
InChI
1S/C7H9N3.2ClH/c8-6-3-1-5(2-4-6)7(9)10;;/h1-4H,8H2,(H3,9,10);2*1H
InChI key
GHEHNICLPWTXJC-UHFFFAOYSA-N
Application
4-二盐酸氨基苯甲脒可用于合成：
- 基于苯甲脒的口服活性纤维蛋白原受体拮抗剂。
- 苯甲脒衍生物，其是选择性和有效的丝氨酸蛋白酶抑制剂。
- 新型吡咯并[3,2-c]喹啉，其是拓扑异构酶抑制剂（例如甲氧檗因和法格罗宁）的结构类似物。
4-二盐酸氨基苯甲脒在亲和层析中可用作配体，用于酶的纯化和固定。
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Design of orally active, non-peptide fibrinogen receptor antagonists. An evolutionary process from the RGD sequence to novel anti-platelet aggregation agents.
Bovy P R, et al.
Bioorganic & Medicinal Chemistry, 2(9), 881-895 (1994)
In vitro blood compatibility of polymeric biomaterials through covalent immobilization of an amidine derivative.
Gouzy M F, et al.
Biomaterials, 25(17), 3493-3501 (2004)
A L Nguyen et al.
Biotechnology and bioengineering, 34(9), 1186-1190 (1989-11-01)
Reactive polymers have been prepared by copolymeriz-ing N-isopropyl acrylamide (NIPAM) with N-acryloxy-succinimide (NASI) or glycidyl methacrylate (GMA). The amino groups of ligands could react with the residues of NASI or GMA and the polymers could be precipitated by temperature and/or
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 857661-10G | 04061833032305 |
| 857661-1G | 04061825769004 |
| 857661-50G | 04061832107608 |