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SDS
745073

N-[(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyloxycarbonyl]-1,8-diamino-3,6-dioxaoctane

for Copper-free Click Chemistry

Manufacturer: Sigma Aldrich

CAS Number: 1263166-93-3

Synonym(S): (1α,8α,9β)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl N-{2-[2-(2-aminoethoxy)ethoxy]ethyl}carbamate, BCN-amine

Select a Size

Pack Size SKU Availability Price
25 MG 745073-25-MG In Stock ₹ 21,097.93
100 MG 745073-100-MG In Stock ₹ 70,297.55

745073 - 25 MG

₹ 21,097.93

In Stock

Quantity

1

Base Price: ₹ 21,097.93

GST (18%): ₹ 3,797.627

Total Price: ₹ 24,895.557

Quality Level

100

form

liquid

composition

carbon content, 62.94% hydrogen content, 8.70% nitrogen content, 8.63%

reaction suitability

reaction type: click chemistryreagent type: linker

functional group

amine

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@]12CCC#CCC[C@]1([H])[C@@H]2COC(NCCOCCOCCN)=O

InChI

1S/C17H28N2O4/c18-7-9-21-11-12-22-10-8-19-17(20)23-13-16-14-5-3-1-2-4-6-15(14)16/h14-16H,3-13,18H2,(H,19,20)/t14-,15+,16-

InChI key

YZGOWXGENSKDSE-MUJYYYPQSA-N

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Description

  • Application: Amine functionalized cyclooctyne derivative. Cyclooctynes are useful in strain-promoted copper-free azide-alkyne cycloaddition reactions. This strained cyclooctyne will react with azide functionalized compounds or biomolecules without the need for a copper catalyst to result in a stable triazole linkage.
  • Packaging: Bottomless glass bottle. Contents are inside inserted fused cone.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Show Difference

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Sigma Aldrich

745073

for Copper-free Click Chemistry...

Quality Level:
100
form:
liquid
composition:
carbon content, 62.94% hydrogen content, 8.70% nitrogen content, 8.63%
reaction suitability:
reaction type: click chemistryreagent type: linker
functional group:
amine
shipped in:
dry ice
storage temp.:
−20°C
SMILES string:
[H][C@@]12CCC#CCC[C@]1([H])[C@@H]2COC(NCCOCCOCCN)=O
InChI:
1S/C17H28N2O4/c18-7-9-21-11-12-22-10-8-19-17(20)23-13-16-14-5-3-1-2-4-6-15(14)16/h14-16H,3-13,18H2,(H,19,20)/t14-,15+,16-
InChI key:
YZGOWXGENSKDSE-MUJYYYPQSA-N

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Sigma Aldrich

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100
form:
crystals
composition:
__
reaction suitability:
__
functional group:
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shipped in:
__
storage temp.:
__
SMILES string:
CC(Cc1ccc(O)c(O)c1)C(C)Cc2ccc(O)c(O)c2
InChI:
1S/C18H22O4/c1-11(7-13-3-5-15(19)17(21)9-13)12(2)8-14-4-6-16(20)18(22)10-14/h3-6,9-12,19-22H,7-8H2,1-2H3
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HCZKYJDFEPMADG-UHFFFAOYSA-N

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SMILES string:
[K]N(C#N)C(=O)OCc1ccccc1
InChI:
1S/C9H8N2O2.K/c10-7-11-9(12)13-6-8-4-2-1-3-5-8;/h1-5H,6H2,(H,11,12);/q;+1/p-1
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HZBHQPNPJVDRMR-UHFFFAOYSA-M

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reaction suitability:
reaction type: Allylationreaction type: C-C Bond Formationreagent type: catalystreaction type: C-H Activationreagent type: diversification reagent
functional group:
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shipped in:
__
storage temp.:
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SMILES string:
CC(C)S(=O)O[Zn]OS(=O)C(C)C
InChI:
1S/2C3H8O2S.Zn/c2*1-3(2)6(4)5;/h2*3H,1-2H3,(H,4,5);/q;;+2/p-2
InChI key:
PEEMMWYYSHSBTQ-UHFFFAOYSA-L