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SnAP Pip Reagent

Synonym(e):

N-(2-Aminoethyl)-N-[(tributylstannyl)methyl]-Boc ester

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Über diesen Artikel

Empirische Formel (Hill-System):
C20H44N2O2Sn
CAS-Nummer:
Molekulargewicht:
463.29
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22


form

liquid

refractive index

n/D 1.4860

density

1.108 g/mL

functional group

amine, carbamate

storage temp.

−20°C

SMILES string

CCCC[Sn](CCCC)(CN(C(OC(C)(C)C)=O)CCN)CCCC

InChI

1S/C8H17N2O2.3C4H9.Sn/c1-8(2,3)12-7(11)10(4)6-5-9;3*1-3-4-2;/h4-6,9H2,1-3H3;3*1,3-4H2,2H3;

InChI key

LGYNPAYNCSWDHV-UHFFFAOYSA-N

Application

SnAP Reagents provide a one-step route, in tandem with various aldehyde substrates, to saturated N-heterocycles. The synthesis of N-heterocycles through SnAP Reagents requires mild reaction conditions, and aldehydes bearing aryl, heteroaryl, glyoxyl, aliphatic, and halogenated groups are well tolerated. This product was introduced in collaboration with the Jeffrey Bode Research Group

Automate your N-heterocycle formation with Synple Automated Synthesis Platform (SYNPLE-SC002)


signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 1

Lagerklasse

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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