所有图片(1)
About This Item
线性分子式:
C6H5CH2ONHCO2C(CH3)3
CAS号:
分子量:
223.27
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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质量水平
方案
99%
mp
45-47 °C (lit.)
官能团
amine
phenyl
SMILES字符串
CC(C)(C)OC(=O)NOCc1ccccc1
InChI
1S/C12H17NO3/c1-12(2,3)16-11(14)13-15-9-10-7-5-4-6-8-10/h4-8H,9H2,1-3H3,(H,13,14)
InChI key
MZNBNPWFHGWAGH-UHFFFAOYSA-N
一般描述
tert-Butyl N-(benzyloxy)carbamate (tert-butyl benzyloxycarbamate), a protected hydroxylamine,[1] is an N-alkyl-N-benzyloxy carbamate.[2] Its C-N cross coupling reaction with fluorescein ditriflate has been reported.[1] It participates in facile intramolecular cyclization with various carbon nucleophiles to afford functionalized 5- and 6-membered protected cyclic hydroxamic acids.[2]
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Synthesis of rhodamines from fluoresceins using Pd-catalyzed C-N cross-coupling.
Grimm JB and Lavis LD.
Organic Letters, 13(24), 6354-6357 (2011)
I Kursula et al.
European journal of biochemistry, 268(19), 5189-5196 (2001-10-09)
The crystal structure of leishmania triosephosphate isomerase (TIM) complexed with 2-(N-formyl-N-hydroxy)-aminoethyl phosphonate (IPP) highlights the importance of Asn11 for binding and catalysis. IPP is an analogue of the substrate D-glyceraldehyde-3-phosphate, and it is observed to bind with its aldehyde oxygen
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