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Merck
CN

358754

1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine, polymer-bound

200-400 mesh, extent of labeling: 2.6 mmol/g loading, 2 % cross-linked with divinylbenzene

Synonym(s):

1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine bound to polystyrene, 1,5,7-Triazabicyclo[4.4.0]dec-5-ene–polystyrene crosslinked with 2% DVB, ‘7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene’ on polystyrene

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About This Item

NACRES:
NA.22
UNSPSC Code:
12352128

Key Documents

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crosslinking

2 % cross-linked with divinylbenzene

reaction suitability

reaction type: solution phase peptide synthesis, reactivity: proton reactive

extent of labeling

2.6 mmol/g loading

particle size

200-400 mesh

Quality Level

200

Related Categories

Features and Benefits

This versatile polymer-bound base has been used as a reusable basic catalyst foe regioselective acylations; as both a base for the deprotonation of phenols and as a scavenger of excess phenil in the synthesis of aryl ethers from phenols; in the addition of dialkyl phosphites to a variety of carbonyl compounds, as well as, serving as a catalyst in the nitroaldol (Henry) reaction; and as a scavenger of activated ester electophiles.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
1453093V
1453093
07614EJ
017331/1
01606JE

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Xu, W.
Tetrahedron Letters, 38, 7337-7337 (1997)
Tamura, Y.
Synthetic Communications, 24, 2907-2907 (1994)

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