
S-Phenyl thioacetate | CAS:934-87-2
S-Phenyl thioacetate
- 名称:S-硫代乙酸苯酯 | S-Phenyl thioacetate
- CAS号:934-87-2
- 别名:
- 分子式:C8H8OS
- 分子量:152.21
- EINESC号:213-294-2
产品描述
物理化学性质
沸点 | 99-100 ºC (6 mmHg) |
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闪点 | 79 ºC |
密度 | 1.124 |
折射率 | 1.57 |
安全数据
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Hydroxylamine-O-sulfonic Acid.Erdik E and Saczewski J. e-EROS Encyclopedia of Reagents for Organic Synthesis. (2013)
A New Strategy for the Preparation of N-Aminopiperidine Using Hydroxylamine-O-Sulfonic Acid: Synthesis, Kinetic Modelling, Phase Equilibria, Extraction and Processes.Labarthe E, et al. Advances in Chemical Engineering and Science, 3(2) (2013)
Mechanism of metal-mediated DNA damage induced by metabolites of carcinogenic 2-nitropropane.K Sakano et al.Mutation research, 479(1-2), 101-111 (2001-07-27)
Co-immobilization of semaphorin3A and nerve growth factor to guide and pattern axons.Aleesha M McCormick et al.Acta biomaterialia, 28, 33-44 (2015-09-24)
Synthesis and molecular structure of (Z)-1H-purin-6-ylideneaminooxysulfonic acid: a possible secondary metabolite of adenine.Saczewski J and Gdaniec M. Heterocyclic Communications, 18(3), 109-112 (2012)
Aminations of guanosine and deoxyguanosine with hydroxylamine-O-sulfonic acid and 2,4-dinitrophenoxyamine. Dependence on the reaction medium.K Kohda et al.Nucleic acids symposium series, (17)(17), 145-148 (1986-01-01)
Amination of tetrazoles with hydroxylamine-O-sulfonic acid: 1-and 2-aminotetrazoles.Raap R. Canadian Journal of Chemistry, 47(19), 3677-3681 (1969)
N-Trinitroethylamino functionalization of nitroimidazoles: a new strategy for high performance energetic materials.Yin P, et al. Journal of Material Chemistry A, 1(25), 7500-7510 (2013)
The reaction of organoboranes with chloramine and with hydroxylamine-O-sulfonic acid. A convenient synthesis of amines from olefins via hydroboration.Brown HC, et al. Journal of the American Chemical Society, 86(17), 3565-3566 (1964)
Elusive metal-free primary amination of arylboronic acids: synthetic studies and mechanism by density functional theory.Chen Zhu et al.Journal of the American Chemical Society, 134(44), 18253-18256 (2012-10-23)
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