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CAS RN: 112022-83-0 | Product Number: D2130
(R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine

Purity: >97.0%(T)
- (R)-3,3-Diphenyl-1-methyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole
- (R)-Me-CBS Catalyst
- (R)-(+)-2-Methyl-CBS-oxazaborolidine
Size | Unit Price | Philadelphia, PA | Portland, OR | Japan* | Quantity |
---|---|---|---|---|---|
1G |
$65.00
|
Contact Us | 1 | 7 |
|
5G |
$227.00
|
Contact Us | Contact Us | 5 |
|
* Items in stock locally ship in 1-2 business days. Items from Japan stock are able to ship from a US warehouse within 2 weeks. Please contact TCI for lead times on items not in stock. Excludes regulated items and items that ship on ice.
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Product Number | D2130 |
Purity / Analysis Method | >97.0%(T) |
Molecular Formula / Molecular Weight | C__1__8H__2__0BNO = 277.17 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Frozen (<0°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Moisture Sensitive,Heat Sensitive |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 112022-83-0 |
Reaxys Registry Number | 9059874 |
PubChem Substance ID | 87568574 |
MDL Number | MFCD00078440 |
Appearance | White to Almost white powder to crystal |
Purity(Nonaqueous Titration) | min. 97.0 % |
Specific rotation [a]20/D | +68.0 to +75.0 deg(C=1, MeOH) |
NMR | confirm to structure |
Specific Rotation | 68° (C=1,MeOH) |
HS Number | 2933.99.7900 |
References
- 1)Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
- 2)A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses
- 3)Enantioselective route to a key intermediate in the total synthesis of ginkgolide B
- 4)Total synthesis of (±)-forskolin
- 5)Total Synthesis of (+)-Lyconadin A and Related Compounds via Oxidative C-N Bond Formation
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