Acetylthiomethyl-diphenylphosphine borane complex
- Product Name
- Acetylthiomethyl-diphenylphosphine borane complex
- CAS No.
- 446822-71-5
- Chemical Name
- Acetylthiomethyl-diphenylphosphine borane complex
- Synonyms
- Acetylthiomethyl-diphenylphosphine borane complex;Acetylthiomethyl-diphenylphosphine borane complex >=98.0%
- CBNumber
- CB42090207
- Molecular Formula
- C15H18BOPS
- Formula Weight
- 288.157
- MOL File
- 446822-71-5.mol
Acetylthiomethyl-diphenylphosphine borane complex Property
- Melting point:
- 52-55 °C
- storage temp.
- 2-8°C
- form
- solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 670359
- Product name
- Acetylthiomethyl-diphenylphosphine borane complex
- Purity
- ≥98.0%
- Packaging
- 250mg
- Price
- $180
- Updated
- 2022/05/15
- Product number
- 670359
- Product name
- Acetylthiomethyl-diphenylphosphine borane complex
- Purity
- ≥98.0%
- Packaging
- 1g
- Price
- $716
- Updated
- 2022/05/15
- Product number
- BOR0003689
- Product name
- ACETYLTHIOMETHYL-DIPHENYLPHOSPHINE BORANE COMPLEX
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.09
- Updated
- 2021/12/16
Acetylthiomethyl-diphenylphosphine borane complex Chemical Properties,Usage,Production
Uses
- Traceless Staudinger ligation reagent with borane protecting group.
- The borane group stabilizes the phosphine against oxidation and can be easily removed with mild basic or acidic conditions to yield the active phosphine.
- After reaction with an azide, the phosphine is eliminated in the presence of water to yield a native amide bond.
- Used in the synthesis of cyclic peptides.
Uses
Traceless Staudinger ligation reagent with borane protecting group. The borane group stabilizes the phosphine against oxidation and can be easily removed with mild basic or acidic conditions to yield the active phosphine. After reaction with an azide, the phosphine is eliminated in the presence of water to yield a native amide bond. Used in the synthesis of cyclic peptides.
reaction suitability
reaction type: click chemistry
reagent type: ligand
reaction type: Staudinger Reaction
Acetylthiomethyl-diphenylphosphine borane complex Preparation Products And Raw materials
Raw materials
Preparation Products
Acetylthiomethyl-diphenylphosphine borane complex Suppliers
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- Country
- United States
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