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Merck
CN

17354

2-(BOC-氨基)溴乙烷

≥97.0% (GC)

别名:

N-(2-溴乙基)氨基甲酸叔丁酯, N-Boc-2-溴乙基胺

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关于此项目

线性分子式:
BrCH2CH2NHCO2C(CH3)3
化学文摘社编号:
分子量:
224.10
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2325117
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产品名称

2-(BOC-氨基)溴乙烷, ≥97.0% (GC)

InChI key

TZRQZPMQUXEZMC-UHFFFAOYSA-N

SMILES string

BrCCNC(OC(C)(C)C)=O

InChI

1S/C7H14BrNO2/c1-7(2,3)11-6(10)9-5-4-8/h4-5H2,1-3H3,(H,9,10)

assay

≥97.0% (GC)

reaction suitability

reagent type: cross-linking reagent

mp

30-32 °C (lit.)

functional group

Boc
amine
bromo

shipped in

wet ice

storage temp.

−20°C

Quality Level

General description

2-(BOC-氨基)溴乙烷在有机合成中可用于引入Boc保护基团,合成多肽等各种化合物。

Other Notes

制备具有亲核和亲电末端的氟化间隔臂的结构单元;合成联苯连接基

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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P. Mougenot et al.
The Journal of Organic Chemistry, 61, 408-408 (1996)
L. Chen et al.
Tetrahedron Letters, 39, 3627-3627 (1998)
Convergent Synthesis and Diversity of Amino Acid Based Dendrimers
Arwin J B, et al.
European Journal of Organic Chemistry, 1903-1915 (2001)
Jinping Cheng et al.
International journal of nanomedicine, 6, 2007-2021 (2011-10-07)
Carbon nanotubes have shown broad potential in biomedical applications, given their unique mechanical, optical, and chemical properties. In this pilot study, carbon nanotubes have been explored as multimodal drug delivery vectors that facilitate antiangiogenic therapy in zebrafish embryos. Three different
Marina Marinović et al.
Molecules (Basel, Switzerland), 25(19) (2020-09-27)
Harmicines represent hybrid compounds composed of β-carboline alkaloid harmine and cinnamic acid derivatives (CADs). In this paper we report the synthesis of amide-type harmicines and the evaluation of their biological activity. N-harmicines 5a-f and O-harmicines 6a-h were prepared by a

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