ChemicalBook--->CAS DataBase List--->1557287-99-6

1557287-99-6

1557287-99-6 Structure

1557287-99-6 Structure
IdentificationBack Directory
[Name]

SnAP Pip Reagent
[CAS]

1557287-99-6
[Synonyms]

SnAP Pip Reagent
N1-Boc-N1-[(tributylstannyl)methyl]-1,2-ethanediamine
tert-Butyl (2-aminoethyl)[(tributylstannyl)methyl]carbamate
Carbamic acid, N-(2-aminoethyl)-N-[(tributylstannyl)methyl]-, 1,1-dimethylethyl ester
[Molecular Formula]

C20H44N2O2Sn
[MDL Number]

MFCD28397085
[MOL File]

1557287-99-6.mol
[Molecular Weight]

463.29
Chemical PropertiesBack Directory
[Boiling point ]

458.3±55.0 °C(Predicted)
[density ]

1.108 g/mL
[refractive index ]

n/D1.4860
[storage temp. ]

-20°C
[form ]

liquid
[pka]

9.42±0.10(Predicted)
[InChI]

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;
[InChIKey]

LGYNPAYNCSWDHV-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)N(CCN)C[Sn](CCCC)(CCCC)CCCC
Safety DataBack Directory
[RIDADR ]

UN 2788 6.1 / PGIII
[WGK Germany ]

WGK 3
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[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
Hazard InformationBack Directory
[Uses]

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
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