Home Categories (R)-3,3′-Bis(2,4,6-triisopropylphenyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate
A7196412

(R)-3,3′-Bis(2,4,6-triisopropylphenyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate , 98% , 791616-63-2

Synonym(s):
(11bR)-4-Hydroxy-2,6-bis[2,4,6-tris(1-methylethyl)phenyl]dinaphtho[2,1-d:1′,2′-f]-1,3,2-dioxaphosphepin 4-oxide;(11bS)-4-Hydroxy-2,6-bis[2,4,6-tris(1-methylethyl)phenyl]dinaphtho[2,1-d:1′,2′-f]-1,3,2-dioxaphosphepin 4-oxide;(R)-3,3′-Bis(2,4,6-triisopropylphenyl)-1,1′-bi-2-naphthol cyclic monophosphate;(R)-TRIP;(S)-3,3′-Bis(2,4,6-triisopropylphenyl)-1,1′-bi-2-naphthol cyclic monophosphate

CAS NO.:791616-63-2

Empirical Formula: C50H57O4P

Molecular Weight: 752.98

MDL number: MFCD10567009

Pack Size Price Stock Quantity
25mg RMB237.60 In Stock
100MG RMB824.80 In Stock
250mg RMB1599.20 In Stock
500MG RMB3000.80 In Stock
1g RMB5919.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Boiling point: 814.2±75.0 °C(Predicted)
Density  1.17±0.1 g/cm3(Predicted)
storage temp.  Inert atmosphere,Room Temperature
pka 1.12±0.20(Predicted)
form  Powder
color  white to light-yellow
InChIKey AGQAQYPGJDBIQR-UHFFFAOYSA-N

Description and Uses

Versatile organocatalyst. Uses include asymmetric reductive amination, enantioselective Diels-Alder reactions and asymmetric counteranion-directed catalysis (ACDC). Can be used in cooperation with chiral iridium complexes to catalyze greener asymmetric reductive amination using hydrogen gas.

Metal-Br?nsted Acid Cooperative Catalysis for Asymmetric Reductive Amination

Safety

Symbol(GHS) 
GHS07
Signal word  Danger
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280-P305+P351+P338-P304+P340-P405-P501A
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
TSCA  No
HS Code  29199000

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