[(1S)-1-Aminoethyl]phosphonic acid（CAS号：66068-76-6）
(S)-(+)-1-氨基乙基膦酸
基本信息
![[(1S)-1-Aminoethyl]phosphonic acid](/structs/660/66068-76-6-6eae.webp "[(1S)-1-Aminoethyl]phosphonic acid")
CAS号
66068-76-6
分子式
C2H8NO3P
分子量
125.06 g/mol
Quick Actions
基本物理性质
熔点
290 °C (dec.) (lit.)
安全信息
查看安全信息危险说明
H315-H319-H335
同义词与参考文献
英文
- J-100032
- CHEBI:136675
- CHEMBL57466
- (S)-(+)-1-Aminoethylphosphonic acid, 99%
- (S)-(+)-(1-aminoethyl)phosphonic acid
- 1-Aminoethylphosphonic acid, (S)-
- Phosphonic acid, (1-aminoethyl)-, (S)-
- UNII-YV7Y1B14AP
- (S)-(1-Aminoethyl)phosphonicacid
- 66068-76-6
- SCHEMBL6662622
- (S)-(1-Aminoethyl)phosphonic acid
- (S)-1-aminoethanephosphonic acid
- PHOSPHONIC ACID, ((1S)-1-AMINOETHYL)-
- [(1S)-1-aminoethyl]phosphonic acid
- PHOSPHONIC ACID, P-((1S)-1-AMINOETHYL)-
- (S)-(+)-1-Aminoethylphosphonic acid
- DTXSID001299163
- YV7Y1B14AP
- AKOS025295605
- (s)-1-aminoethyl phosphonic acid
- D-Ala(P)
- Q27294731
- (s)-1-aminoethylphosphonic acid
- J282.316K
- Phosphonic acid,P-[(1S)-1-aminoethyl]-
- (S)-(+)-1-Phosphonoethylamine
- (S)-(+)-(1-AMINOETHYL)PHOSPHONIC ACID
- (S)-(1-Aminoethyl)phosphonsaeure
- (S)-1-aminoethyl phosphonic acid
- D-(+)-1-Aminoethylphosphonic acid
中文
- (S)-(+)-(1-氨基乙基)磷酸
- (S)-(+)-1-氨基乙基膦酸
- D-(+)-1-氨基乙基膦酸
MDL_Number
MFCD00066503
CAS号
66068-76-6
Customs_Code
2931900090
供应商信息
| 供应商名称 | 会员等级 | 认证状态 | 主要类别 | 最小订购量 | 操作 |
|---|---|---|---|---|---|
 中国 - 上海阿拉丁生化科技股份有限公司 |
|||||
 印度尼西亚 - Van Aroma |
|||||
 墨西哥 - 墨西哥国际实验室供应商，SA de C.V. |
|||||
| 中国 - 成都遨帆医药科技有限公司 |
|||||
| 中国 - 常州市科威精细化工有限公司 |
|||||
 法国 - Teclis SAS |
|||||
 德国 - 哈顿Anlagentechnik GmbH |
|||||
 萨尔瓦多 - 商业与代理公司 |
![224-53-3 - 二苯并[C,H]吖啶](/structs/224/224-53-3-97c9.webp "224-53-3 - 二苯并[C,H]吖啶")
期刊推荐
Corrosion Science
Canadian Metallurgical Quarterly
Journal of the American Chemical Society
Biopolymers
Journal of the Chinese Chemical Society
Bulletin of the Chemical Society of Japan
Ferroelectrics
Anti-Corrosion Methods and Materials
Advances in Colloid and Interface Science
Chemistry of Heterocyclic Compounds
相关文献
Increasing efficiency of perovskite solar cells using low concentrating photovoltaic systems
Hasan Baig, Hiroyuki Kanda, Abdullah M. Asiri, Mohammad Khaja Nazeeruddin, Tapas Mallick
DOI: 10.1039/C9SE00550A
Biomaterials Science Emerging Investigators 2021
Maria E. Southall
DOI: 10.1039/D1BM90053F
Selective light driven reduction of CO2 to HCOOH in water using a {MoV9}n (n = 1332–3600) based soft-oxometalate (SOM)
DOI: 10.1039/C7CC09520A
Palladium-catalyzed silaborative carbocyclizations of 1,6-diynes
Qian Zhang, Qiu-Ju Liang, Jian-Lin Xu, Yun-He Xu
DOI: 10.1039/C8CC00097B
A model-based comparison of Ru and Ni catalysts for the Sabatier reaction
DOI: 10.1039/C9SE00787C
An elemental S/P photocatalyst for hydrogen evolution from water under visible to near-infrared light irradiation
Qiuyan Cao, Minna Guo, Jing Cao, Haili Lin, Yong Chen, Shifu Chen
DOI: 10.1039/C9CC05952K
Efficient one-pot synthesis of alkyl levulinate from xylose with an integrated dehydration/transfer-hydrogenation/alcoholysis process
Mengmeng Wang, Xueying Gao, Liang He, Junhua Zhang
DOI: 10.1039/C9SE00982E
Catalytic depolymerization of Kraft lignin to produce liquid fuels via Ni–Sn metal oxide catalysts
Baikai Zhang, Wenzhi Li, Xiaomeng Dou, Jindong Wang, Lele Jin, Ajibola T. Ogunbiyi, Xiaosen Li
DOI: 10.1039/C9SE01089K