84012-00-0 Usage
Molecular Weight
181.19 g/mol
Structure
A bicyclic compound containing a seven-membered ring with a nitrogen atom and a carboxylic acid group.
Functional Groups
Carboxylic acid, ester, and a double bond with cis configuration.
Stereochemistry
Cis configuration around the double bond.
Application
Used as a building block in organic synthesis and pharmaceutical research.
Biological Activity
Potentially valuable biological activities due to its versatile structure.
Safety Considerations
Specific handling and safety considerations may be required due to its chemical nature and potential reactivity.
Solubility
Soluble in organic solvents like methanol, ethanol, and acetone.
Stability
Stable under normal temperature and pressure conditions, but sensitive to heat, light, and moisture.
Reactivity
May react with strong acids, strong bases, and nucleophiles.
Synthesis
Can be synthesized through various methods, such as cyclization reactions and functional group transformations.
Derivatives
Can be further modified to create a variety of biologically active compounds.
Purity
Typically characterized by techniques like NMR, mass spectrometry, and elemental analysis.
Storage
Should be stored in a cool, dry, and well-sealed container, away from light and heat sources.
Check Digit Verification of cas no
The CAS Registry Mumber 84012-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,1 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84012-00:
(7*8)+(6*4)+(5*0)+(4*1)+(3*2)+(2*0)+(1*0)=90
90 % 10 = 0
So 84012-00-0 is a valid CAS Registry Number.
84012-00-0Relevant articles and documents
SYNTHESIS OF 3,5-TRANS-3-METHOXYCARBONYL-1-CARBAPENAM FROM METHYL (+/-)-PYROGLUTAMATE
Nagasaka, Tatsuo,Tsukada, Atsuhiko,Hamaguchi, Fumiko
, p. 2015 - 2022 (2007/10/02)
Synthesis of 3,5-trans-3-methoxycarbonyl-1-carbapenam in six steps from methyl (+/-)-pyroglutamate is described.
