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Merck
CN

695718

(R)-3,3′-Bis(9-anthracenyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate

95%

Synonym(s):

(11bR)-2,6-Di-9-anthracenyl-4-hydroxy-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-oxide

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About This Item

Empirical Formula (Hill Notation):
C48H29O4P
CAS Number:
361342-51-0
Molecular Weight:
700.72
MDL number:
MFCD29073238
UNSPSC Code:
12352005
PubChem Substance ID:
329761763
NACRES:
NA.22

Key Documents

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Product Name

(R)-3,3′-Bis(9-anthracenyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate, 95%

SMILES string

OP1(=O)Oc2c(cc3CCC=Cc3c2-c4c(O1)c(cc5ccccc45)-c6c7ccccc7cc8ccccc68)-c9c%10ccccc%10cc%11ccccc9%11

InChI

1S/C48H31O4P/c49-53(50)51-47-41(43-35-19-7-1-13-29(35)25-30-14-2-8-20-36(30)43)27-33-17-5-11-23-39(33)45(47)46-40-24-12-6-18-34(40)28-42(48(46)52-53)44-37-21-9-3-15-31(37)26-32-16-4-10-22-38(32)44/h1-5,7-17,19-28H,6,18H2,(H,49,50)

InChI key

SZKDXDJLUYHXLW-UHFFFAOYSA-N

assay

95%

form

solid

mp

288-292 °C (D)

functional group

phosphate

storage temp.

−20°C

Quality Level

100

Related Categories

Application

Catalyst used in asymmetric direct alkylation of α-diazoester via C-H bond cleavage.
Catalysts used in enantioselective condensation/amine addition reactions

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS9967
MKCM4629
MKBX5319V
MKBJ8065V
MKBG2357V

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Asymmetric Brønsted acid catalysis: catalytic enantioselective synthesis of highly biologically active dihydroquinazolinones.
Magnus Rueping et al.
Angewandte Chemie (International ed. in English), 48(5), 908-910 (2008-12-23)
Daisuke Uraguchi et al.
Journal of the American Chemical Society, 127(26), 9360-9361 (2005-06-30)
A new variant of phosphoric acid-catalyzed C-C bond forming reaction, direct alkylation of alpha-diazoester, via C-H bond cleavage is presented. The resulting products, beta-amino-alpha-diazoesters, are highly functionalized and useful synthetic precursors for various types of beta-amino acids.

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