166520-22-5
Post Buying Request-
-
Basic information
- Product Name: 2,5-Diazabicyclo[2.2.1]heptane-2-acetamide, N-(2,6-dimethylphenyl)-, (1S,4S)-
- Synonyms:
- CAS NO:166520-22-5
- Molecular Formula: C15H21N3O
- Molecular Weight:
- EINECS: N/A
- Product Categories: N/A
- Mol File: 166520-22-5.mol
- Article Data: 0
-
Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 2,5-Diazabicyclo[2.2.1]heptane-2-acetamide, N-(2,6-dimethylphenyl)-, (1S,4S)-(CAS DataBase Reference)
- NIST Chemistry Reference: 2,5-Diazabicyclo[2.2.1]heptane-2-acetamide, N-(2,6-dimethylphenyl)-, (1S,4S)-(166520-22-5)
- EPA Substance Registry System: 2,5-Diazabicyclo[2.2.1]heptane-2-acetamide, N-(2,6-dimethylphenyl)-, (1S,4S)-(166520-22-5)
-
Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 166520-22-5(Hazardous Substances Data)
166520-22-5 Suppliers
Recommended suppliersmore
166520-22-5 Usage
Chemical Category
AcetamidesThis compound belongs to a class of organic compounds that have a core structure of an amide group attached to an acetic acid derivative.
Derivation
2,5-Diazabicyclo[2.2.1]heptane and N-(2,6-dimethylphenyl)acetic acidThe compound is synthesized by combining these two precursors, resulting in the formation of the desired product.
Stereochemistry
(1S,4S)-The stereochemistry of the compound refers to the spatial arrangement of its atoms. In this case, the (1S,4S)notation indicates the specific configuration of the molecule, which is important for its reactivity and properties.
Pharmaceutical Industry Application
Building Block in Drug SynthesisThis compound is commonly used as an intermediate in the synthesis of various drugs, providing a foundation for the development of new pharmaceuticals.
Unique Structure and Reactivity
Valuable in Organic Synthesis ProcessesThe compound's structure and reactivity make it a valuable intermediate in organic synthesis, allowing for the creation of a wide range of chemical products.
Potential as a Chiral Ligand in Asymmetric Catalysis
The compound has demonstrated potential as a chiral ligand, which can be used in asymmetric catalysis to create enantiomerically pure products. This is important in the pharmaceutical industry, as the desired biological activity is often associated with a specific enantiomer.Diverse Applications
Pharmaceuticals and Organic ChemistryThe compound has a variety of applications in both the pharmaceutical industry and organic chemistry, making it a versatile and important chemical intermediate.
Check Digit Verification of cas no
The CAS Registry Mumber 166520-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,5,2 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.Calculate Digit Verification of CAS Registry Number 166520-22:
(8*1)+(7*6)+(6*6)+(5*5)+(4*2)+(3*0)+(2*2)+(1*2)=125
125 % 10 = 5
So 166520-22-5 is a valid CAS Registry Number.
166520-22-5Upstream product
166520-22-5Downstream Products
Post a RFQ
1
What can I do for you?
Get Best Price
Get Best Price for 166520-22-5
2,5-Diazabicyclo[2.2.1]heptane-2-acetamide, N-(2,6-dimethylphenyl)-,
(1S,4S)-
