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Merck
CN

677191

(R)-(+)-α,α-二苯基-2-吡咯烷甲醇三甲基硅基醚

96%

别名:

(2R)-2-[二苯基[(三甲基硅基)氧基]甲基]吡咯烷, (R)-α,α-二苯基脯氨醇三甲基硅基醚, (R)-2-[Diphenyl(trimethylsilanyloxy)methyl]pyrrolidine

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关于此项目

经验公式(希尔记法):
C20H27NOSi
化学文摘社编号:
分子量:
325.52
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
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产品名称

(R)-(+)-α,α-二苯基-2-吡咯烷甲醇三甲基硅基醚, 96%

InChI

1S/C20H27NOSi/c1-23(2,3)22-20(19-15-10-16-21-19,17-11-6-4-7-12-17)18-13-8-5-9-14-18/h4-9,11-14,19,21H,10,15-16H2,1-3H3/t19-/m1/s1

SMILES string

C[Si](C)(C)OC([C@H]1CCCN1)(c2ccccc2)c3ccccc3

InChI key

RSUHWMSTWSSNOW-LJQANCHMSA-N

assay

96%

form

solid

optical activity

[α]22/D +52±5°, c = 1 in chloroform

refractive index

n20/D 1.5509

density

1.0459 g/mL at 25 °C

functional group

phenyl

storage temp.

2-8°C

Quality Level

Application

(R)-(+)-α,α-Diphenyl-2-pyrrolidinemethanol trimethylsilyl ether can be used as a catalyst to synthesize:
  • Glycofused tricyclic derivatives, which are used in the development of amyloid β-peptide diagnostic tools.
  • Cyclohexene carbaldehyde derivatives by reacting benzoylnitromethane with aliphatic enals.

General description

(R)-(+)-α,α-Diphenyl-2-pyrrolidinemethanol trimethylsilyl ether is a diarylprolinol silyl ether organocatalyst.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Synthesis and Preliminary Biological Evaluation of Fluorescent Glycofused Tricyclic Derivatives of Amyloid β-Peptide Ligands
D'Orazio G, et al.
European Journal of Organic Chemistry, 2016(9), 1660-1664 (2016)
Organocatalytic Cascade Reaction of Aliphatic Enals and Benzoylnitromethane: Synthesis of Enantioenriched Tetrasubstituted Cyclohexene Carbaldehyde
David Rodriguez FA, et al.
Journal of Chemistry, 2020 (2020)
The diarylprolinol silyl ether system: a general organocatalyst.
Jensen KL, et al.
Accounts of Chemical Research, 45(2), 248-264 (2011)

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