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Merck

407690

Sigma-Aldrich

N-(苄氧基)氨基甲酸叔丁酯

99%

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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:

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]

应用

tert-Butyl N-(benzyloxy)carbamate was used in the preparation of seven-membered cyclic hydroxamic acids.[2] It may be used in the synthesis of 2-(N-formyl-N-hydroxyamino) ethylphosphonate (IPP).[3]

象形图

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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


历史批次信息供参考:

分析证书(COA)

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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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