24850-33-7

24850-33-7
24850-33-7
24850-33-7

24850-33-7

Min.Order / FOB Price:Get Latest Price

100 Kilogram

Negotiable

  • Min.Order :100 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram,Other

Keywords

RARECHEM AH PB 0251 24850-33-7 C15H32Sn

Quick Details

  • Appearance:powder
  • Application:24850-33-7
  • PackAge:Depended
  • ProductionCapacity:300|Kilogram|Month
  • Storage:Refrigerator
  • Transportation:by air or by sea

Superiority:

Allyltributyltin Basic information
Product Name: Allyltributyltin
Synonyms: ALLYLTRIBUTYLSTANNANE;ALLYLTRIBUTYLTIN;ALLYLTRIBUTYLTIN(IV);ALLYLTRI-N-BUTYLTIN;TRIBUTYL-2-PROPENYLSTANNANE;Stannane, tributyl-2-propenyl-;Allytri-N-Butyltin;Allyltri-n-butyltin,97%
CAS: 24850-33-7
MF: C15H32Sn
MW: 331.12
EINECS: 246-494-3
Product Categories: Alkyl Metals;Sn (Tin) Compounds;Classes of Metal Compounds;Grignard Reagents & Alkyl Metals;Synthetic Organic Chemistry;Typical Metal Compounds;Organometallic Reagents;Organotin;Organotins;Stannanes;Chemical Synthesis;Organometallic Reagents
Mol File: 24850-33-7.mol
Allyltributyltin Structure
 
Allyltributyltin Chemical Properties
bp  88-92 °C0.2 mm Hg(lit.)
density  1.068 g/mL at 25 °C(lit.)
refractive index  n20/D 1.486(lit.)
Fp  >230 °F
storage temp.  2-8°C
Sensitive  Air Sensitive
BRN  3588340
CAS DataBase Reference 24850-33-7(CAS DataBase Reference)
NIST Chemistry Reference Allyltributyltin(24850-33-7)
 
Safety Information
Hazard Codes  T,N
Risk Statements  21-25-36/38-48/23/25-50/53-23/24/25
Safety Statements  35-36/37/39-45-60-61-28-27-26
RIDADR  UN 2788 6.1/PG 2
WGK Germany  3
13
TSCA  No
HazardClass  6.1
PackingGroup  II
MSDS Information
Provider Language
Tributyl-2-propenylstannane English
SigmaAldrich English
ACROS English
ALFA English
 
Allyltributyltin Usage And Synthesis
Chemical Properties CLEAR COLOURLESS LIQUID
Usage Allylation reagent for aldehydes catalyzed by chiral Lewis acids1,2 and ytterbium(III) trifluoromethanesulfonate (cat. no. 430595).3 Undergoes tetrakis(triphenylphosphine)palladium(0) (cat. no. 216666) catalyzed coupling with iodoquinones4 and allyl acetates.5,6Efficient allylation of aldehydes leading to homoallylic alcohols with trichloro-1,3,5-triazene.7
 
 
 

 

 

 

 

 

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