Home Categories Chemical Reagents 1,1'-(Azodicarbonyl)dipiperidine
A0739412

1,1'-(Azodicarbonyl)dipiperidine , >98.0% , 10465-81-3

Synonym(s):
1,1′-Azobis(N,N-pentamethyleneformamide);ADD;Azodicarboxylic acid dipiperidide;NSC 356027;SR 4077

CAS NO.:10465-81-3

Empirical Formula: C12H20N4O2

Molecular Weight: 252.31

MDL number: MFCD00010111

Pack Size Price Stock Quantity
1G RMB24.00 In Stock
5G RMB88.80 In Stock
25G RMB312.80 In Stock
100G RMB960.80 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 132-136 °C(lit.)
Boiling point: 366.4±25.0 °C(Predicted)
Density  1.29±0.1 g/cm3(Predicted)
storage temp.  Keep in dark place,Sealed in dry,Room Temperature
solubility  DMSO (Slightly), Methanol (Slightly), insol petroleum ether; sol ethanol, ether, THF
form  solid
pka -0?+-.0.20(Predicted)
color  yellow
Water Solubility  Slightly soluble in water.
BRN  261917
InChI InChI=1S/C12H20N4O2/c17-11(15-7-3-1-4-8-15)13-14-12(18)16-9-5-2-6-10-16/h1-10H2
InChIKey OQJBFFCUFALWQL-UHFFFAOYSA-N
SMILES N(C(N1CCCCC1)=O)=NC(N1CCCCC1)=O
CAS DataBase Reference 10465-81-3(CAS DataBase Reference)

Description and Uses

1,1''-(Azodicarbonyl)dipiperidine (ADDP) is a reagent commonly used in the Mitsunobu reaction for the condensation of an alcohol and an acidic compound. It has been used as a reagent in the synthesis of G protein-coupled receptor 120 (GPR120) agonists with antidiabetic activity and peroxisome proliferator-activated receptor α (PPARα), PPARγ, and PPARδ triple agonists.

It is used in a study of the copper-catalyzed addition of aryboronic acids to azodicarboxyl derivatives providing aryl-substituted hydrazides. It is widely used reagent for the Mitsunobu reaction. It is reactant for preparation of polyfluoroalkylated tripyrazolylmethane ligands, (-)-Hygromycin A via Mitsunobu glycosylation, optically active α,α-disubstituted amino acids via Mitsunobu reaction, aza-β-lactams through [2+2] cycloaddition reactions, glycosyl disulfides, pyridine ether PPAR agonists, S-glycosyl amino acid, building blocks for combinatorial neoglycopeptide synthesis and is a histamine H3 receptor antagonists. It is a reactant for Mitsunobu inversion reactions.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
RIDADR  3234
WGK Germany  3
TSCA  No
HS Code  29339900

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