所有图片(1)
About This Item
线性分子式:
C6H5NHCH2CH2OH
CAS号:
分子量:
137.18
Beilstein:
774672
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽密度
>1 (vs air)
质量水平
蒸汽压
<0.01 mmHg ( 20 °C)
方案
98%
表单
liquid
折射率
n20/D 1.578 (lit.)
沸点
278-282 °C/760 mmHg (lit.)
密度
1.094 g/mL at 25 °C (lit.)
SMILES字符串
OCCNc1ccccc1
InChI
1S/C8H11NO/c10-7-6-9-8-4-2-1-3-5-8/h1-5,9-10H,6-7H2
InChI key
MWGATWIBSKHFMR-UHFFFAOYSA-N
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应用
N-（2-羟乙基）苯胺被用作人嗅觉UDP-葡糖醛酸糖基转移酶的底物。
警示用语：
Danger
危险分类
Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - STOT RE 2 - STOT SE 1
靶器官
Blood, Blood,hematopoietic system
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
Mercedes Amat et al.
The Journal of organic chemistry, 69(25), 8681-8693 (2004-12-04)
The stereochemical outcome of the conjugate addition of a variety of stabilized nucleophiles (2-indoleacetic enolates and sulfur-stabilized anions) to the phenylglycinol-derived unsaturated lactams trans-2, cis-2, and its 8-ethyl-substituted analogue 10 is studied. The factors governing the exo or endo facial
Mercedes Amat et al.
The Journal of organic chemistry, 72(12), 4431-4439 (2007-05-10)
The stereochemical outcome of the enolate dialkylation of simple phenylglycinol-derived oxazolopiperidone lactams is studied. High stereoselectivities in the generation of the quaternary stereocenter are obtained by the appropriate choice of both the configuration of the starting lactam and the order
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Molecular brain, 1, 16-16 (2008-11-20)
Phenylethanolamines selectively bind to NR2B subunit-containing N-methyl-D-aspartate-subtype of ionotropic glutamate receptors and negatively modulate receptor activity. To investigate the structural and functional properties of the ifenprodil binding domain on the NR2B protein, we have purified a soluble recombinant rat NR2B
Mercedes Amat et al.
The Journal of organic chemistry, 73(17), 6920-6923 (2008-08-01)
A synthetic route to enantiopure cis-2,4-disubstituted and 2,4-bridged piperidines is reported, the key step being a stereoselective conjugate addition of an organocuprate to a phenylglycinol-derived unsaturated lactam bearing a substituent at the 8a-position.
Santos Fustero et al.
The Journal of organic chemistry, 74(11), 4429-4432 (2009-05-15)
The preparation of cyclic dipeptide mimetics from chiral imino lactones derived from (R)-phenylglycinol is described. Key steps of the synthetic route included the fully stereoselective construction of a quaternary center, the formation of six-, seven-, or eight-membered lactams by means
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