3-[(Tributylstannyl)methoxy]-1-propanamine

Suppliers

Names

[ CAS No. ]:
1577233-70-5

[ Name ]:
3-[(Tributylstannyl)methoxy]-1-propanamine

[Synonym ]:
1-Propanamine, 3-[(tributylstannyl)methoxy]-
3-[(Tributylstannyl)methoxy]-1-propanamine
SnAP OA Reagent
MFCD28579830
S167606
3-((Tributylstannyl)methoxy)propan-1-amine

Chemical & Physical Properties

[ Density]:
1.102 at 25℃

[ Boiling Point ]:
387.6±48.0 °C at 760 mmHg

[ Molecular Formula ]:
C16H37NOSn

[ Molecular Weight ]:
378.18

[ Flash Point ]:
188.2±29.6 °C

[ Exact Mass ]:
379.189728

[ LogP ]:
7.75

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Storage condition ]:
-20℃

Safety Information

[ Symbol ]:

GHS06, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301 + H311 + H331-H315-H319-H335-H410

[ Precautionary Statements ]:
P261-P273-P280-P301 + P310-P305 + P351 + P338-P311

[ RIDADR ]:
UN 2788 6.1 / PGIII

Articles

SnAP reagents for the transformation of aldehydes into substituted thiomorpholines--an alternative to cross-coupling with saturated heterocycles.

Angew. Chem. Int. Ed. Engl. 52(6) , 1705-8, (2013)

SnAP reagents for the one-step synthesis of medium-ring saturated N-heterocycles from aldehydes.

Nature Chemistry 6(4) , 310-4, (2014)

Interest in saturated N-heterocycles as scaffolds for the synthesis of bioactive molecules is increasing. Reliable and predictable synthetic methods for the preparation of these compounds, especially ...

One-step synthesis of saturated spirocyclic N-heterocycles with stannyl amine protocol (SnAP) reagents and ketones.

J. Am. Chem. Soc. 136(51) , 17726-9, (2014)

The combination of cyclic ketones and stannyl amine protocol (SnAP) reagents affords saturated, spirocyclic N-heterocycles under operationally simple reaction conditions. The resulting, N-unprotected ...


More Articles


Related Compounds

  • 2-{[(2S,3S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]oxy}-3-methoxypropanoic acid
  • 1-[2-(cyclopropylmethyl)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-3,3-dimethylazetidine-2-carboxylic acid
  • 2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]-2-methylcyclohexane-1-carboxylic acid
  • 2-[(2S,3R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methoxybutanamido]-2-methylpentanoic acid
  • 2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1,3-thiazole-5-carbonyl]-5-oxopyrazolidine-3-carboxylic acid
  • rac-1-[(1R,2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclohexaneamido]cyclopropane-1-carboxylic acid
  • rac-4-{1-[(1R,2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclohexyl]-N-methylformamido}butanoic acid
  • 3-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3,3-dimethyl-N-propylbutanamido]propanoic acid
  • 4-{1-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopent-1-ene-1-carbonyl]azetidin-3-yl}butanoic acid
  • 4-{1-[(2R,3S)-3-(benzyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoyl]azetidin-3-yl}butanoic acid
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.