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Merck

53175

Sigma-Aldrich

N-Boc-间苯二胺

≥98.0% (HPLC)

别名:

3-(叔丁氧羰基氨基)苯胺, 叔丁基-3-氨苯基氨基甲酸酯

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About This Item

经验公式(希尔记法):
C11H16N2O2
CAS号:
分子量:
208.26
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥98.0% (HPLC)

反應適用性

reagent type: cross-linking reagent

官能基

Boc
amine

SMILES 字串

NC1=CC(NC(OC(C)(C)C)=O)=CC=C1

InChI

1S/C11H16N2O2/c1-11(2,3)15-10(14)13-9-6-4-5-8(12)7-9/h4-7H,12H2,1-3H3,(H,13,14)

InChI 密鑰

IEUIEMIRUXSXCL-UHFFFAOYSA-N

應用

N-Boc-m-phenylenediamine (tert-Butyl-3-aminophenylcarbamate) may be used in the preparation of:
  • 5,5′-(propane-2,2-diyl)bis(N-(3-aminophenyl)-4-methyl-3-phenyl-1H-pyrrole-2-carboxamide)
  • ethyl 4-[{3-[(tert-butoxycarbonyl)amino]phenyl}amino]-2-chloropyrimidine-5-carboxylate
  • ethyl 4-(3-(tert-butoxycarbonyl)phenylamino)-2-(methylthio)pyrimidine-5-carboxylate

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Pyrimido [4,5-d] pyrimidin-4(1H)-one Derivatives as Selective Inhibitors of EGFR Threonine790 to Methionine790 (T790M) Mutants.
Xu T, et al.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 125(32), 8545-8548 (2013)
Design, synthesis, and biological evaluation of novel conformationally constrained inhibitors targeting epidermal growth factor receptor threonine790? methionine790 mutant.
Chang S, et al.
Journal of Medicinal Chemistry, 55(6), 2711-2723 (2012)
Grigory V Kolesnikov et al.
Organic & biomolecular chemistry, 9(21), 7358-7364 (2011-09-07)
The design and synthesis of a neutral macrocyclic host that is capable of perrhenate and pertechnetate recognition is described. The anion affinities and underlying coordination modes were estimated by several experimental and theoretical methods including a new technique--reverse (99)Tc NMR

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