89019-23-8 Usage
Chemical Structure
Bicyclic amidine
Usage
a. Base in organic synthesis reactions
b. Catalyst in chemical transformations
c. Ligand for metal-catalyzed reactions
Applications
a. Formation of carbon-carbon and carbon-nitrogen bonds
b. Synthesis of various drug molecules in the pharmaceutical industry
Safety Precautions
Toxic and harmful if not used properly, requires careful handling
Physical Properties
Not provided in the material
Chemical Properties
Not provided in the material
Reactivity
Not provided in the material
Stability
Not provided in the material
Solubility
Not provided in the material
Melting Point
Not provided in the material
Boiling Point
Not provided in the material
Density
Not provided in the material
Molecular Weight
Not provided in the material
Appearance
Not provided in the material
Odor
Not provided in the material
Purity
Not provided in the material
Storage Conditions
Not provided in the material
Regulatory Information
Not provided in the material
Check Digit Verification of cas no
The CAS Registry Mumber 89019-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,1 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89019-23:
(7*8)+(6*9)+(5*0)+(4*1)+(3*9)+(2*2)+(1*3)=148
148 % 10 = 8
So 89019-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N3O/c1-7-5(10)6-3-2-4-9(6)8-6/h8H,2-4H2,1H3,(H,7,10)
89019-23-8Relevant articles and documents
ASYMMETRICAL NITROGEN. 51. SYNTHESIS AND OPTICAL ACTIVATION OF 1,6-DIAZABICYCLOHEXANE-5-CARBOXYLIC ACID AND ITS DERIVATIVES
Shustov, G. V.,Denisenko, S. N.,Zolotoi, A. B.,D'yachenko, O. A.,Atovmyan, L. O.,Kostyanovskii, R. G.
, p. 2071 - 2076 (2007/10/02)
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1,2-Acyl Migration to an Electron-deficient Nitrogen Atom: a New Rearrangement of Diaziridines without Ring Opening
Denisenko, Sergei N.,Shustov, Gennady V.,Kostyanovsky, Remir G.
, p. 1275 - 1276 (2007/10/02)
5-Acyl-1,6-diazabicyclohexane (1) on treatment with t-butyl hypochlorite affords the corresponding N-chloro-derivative (2) which rearranges easily into 6-acyl-5-chloro-1,6-diazabicyclohexane (3) with a 1,2-shift of the acyl group.
