(S,S)-I-PR-DUPHOS
Reaction- Product Name
- (S,S)-I-PR-DUPHOS
- CAS No.
- 147253-69-8
- Chemical Name
- (S,S)-I-PR-DUPHOS
- Synonyms
- (S,S)-I-PR-DUPHOS;(?)-1,2-Bis[(2S,5S)-2,5-diisopropylphospholano]benzene;(-)-1,2-Bis[(2S,5S)-2,5-diisopropylphospholano]benzene;1,2-bis((2S,5S)-2,5-diisopropylphospholan-1-yl)benzene;(-)-1,2-BIS((2S,5S)-2,5-DIISOPROPYLPHOSPHOLANO)BENZENE;(-)-1,2-BIS((2S,5S)-2,5-DI-I-PROPYLPHOSPHOLANO)BENZENE;1,2-Bis[(2S,5S)-2,5-diisopropyl-1-phospholanyl]benzene, 97+%;(-)-1,2-Bis[(2S,5S)-2,5-diisopropylphospholano]benzene, Kanata purity;(-)-1,2-Bis((2S,5S)-2,5-di-i-propylphospholano)benzene (S,S)-i-Pr-DUPHOS;(-)-1,2-Bis((2S,5S)-2,5-di-i-propylphospholano)benzene,98+%(S,S)-i-Pr-DUPHOS
- CBNumber
- CB7128464
- Molecular Formula
- C26H44P2
- Formula Weight
- 418.58
- MOL File
- 147253-69-8.mol
(S,S)-I-PR-DUPHOS Property
- Melting point:
- 40°C
- alpha
- -85° (c 1, hexane)
- Boiling point:
- 502.0±20.0 °C(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- crystal
- color
- white
- Sensitive
- Air Sensitive
Safety
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- WGK Germany
- 3
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H302Harmful if swallowed
H312Harmful in contact with skin
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P312Call a POISON CENTER or doctor/physician if you feel unwell.
P321Specific treatment (see … on this label).
P322Specific measures (see …on this label).
P330Rinse mouth.
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P362Take off contaminated clothing and wash before reuse.
P363Wash contaminated clothing before reuse.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- 668176
- Product name
- (?)-1,2-Bis[(2S,5S)-2,5-diisopropylphospholano]benzene
- Purity
- kanata purity
- Packaging
- 100mg
- Price
- $125
- Updated
- 2023/06/20
- Product number
- H60407
- Product name
- 1,2-Bis[(2S,5S)-2,5-diisopropyl-1-phospholanyl]benzene, 97+%
- Packaging
- 250mg
- Price
- $137
- Updated
- 2021/12/16
- Product number
- H60407
- Product name
- 1,2-Bis[(2S,5S)-2,5-diisopropyl-1-phospholanyl]benzene, 97+%
- Packaging
- 1g
- Price
- $429
- Updated
- 2021/12/16
- Product number
- 15-0411
- Product name
- (-)-1,2-Bis((2S,5S)-2,5-di-i-propylphospholano)benzene, 98+% (S,S)-i-Pr-DUPHOS
- Packaging
- 100mg
- Price
- $82
- Updated
- 2024/03/01
- Product number
- 15-0411
- Product name
- (-)-1,2-Bis((2S,5S)-2,5-di-i-propylphospholano)benzene, 98+% (S,S)-i-Pr-DUPHOS
- Packaging
- 500mg
- Price
- $283
- Updated
- 2024/03/01
(S,S)-I-PR-DUPHOS Chemical Properties,Usage,Production
Reaction
- The DUPHOS family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. Efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides.
- Forms superior catalysts for asymmetric reductive aminations.
- Catalyst used for the asymmetric hydrogenation of enol phosphonates.
- A novel enantioselective synthesis of β-amino alcohols and 1,2-diamines.
- Ligand for the catalytic asymmetric [4+1] cycloaddition of vinylallenes with CO.
- Ligand for the Rh-catalyzed asymmetric enyne cycloisomerization.
- Catalytic enantioselective addition of dialkylzinc to N-Diphenylphosphinoylimines.
- Palladium catalyzed asymmetric phosphination.
- Catalytic enantioselective allylation of ketones.
- Enantioselective synthesis of cyclopropylborates.
- Ligand used in gold catalyzed rearrangement of cyclopropylidene.
(S,S)-I-PR-DUPHOS Preparation Products And Raw materials
Raw materials
Preparation Products
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