(1R,2R)-N,N-dimethylcyclopentane-1,2-diamine is a chiral diamine cyclopentane derivative with the molecular formula C7H16N2. It features two amino groups and two methyl groups attached to the nitrogen atoms, giving it a unique structure. The (1R,2R) designation denotes its specific stereochemistry, which is crucial for its applications.
942492-63-9
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Basic information
- Product Name: (1R,2R)-N,N-dimethylcyclopentane-1,2-diamine
- Synonyms: (1R,2R)-N,N-dimethylcyclopentane-1,2-diamine
- CAS NO:942492-63-9
- Molecular Formula:
- Molecular Weight: 128.217
- EINECS: N/A
- Product Categories: N/A
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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: (1R,2R)-N,N-dimethylcyclopentane-1,2-diamine(CAS DataBase Reference)
- NIST Chemistry Reference: (1R,2R)-N,N-dimethylcyclopentane-1,2-diamine(942492-63-9)
- EPA Substance Registry System: (1R,2R)-N,N-dimethylcyclopentane-1,2-diamine(942492-63-9)
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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: 942492-63-9(Hazardous Substances Data)
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942492-63-9 Usage
Uses
Used in Coordination Chemistry:(1R,2R)-N,N-dimethylcyclopentane-1,2-diamine serves as a ligand in coordination chemistry, particularly for the synthesis of complex metal compounds. Its unique structure and chiral nature contribute to its effectiveness in this application.
Used in Catalysis:
(1R,2R)-N,N-dimethylcyclopentane-1,2-diamine is utilized in catalysis due to its ability to form stable complexes with metal ions, which can enhance the catalytic activity in various chemical reactions.
Used in Asymmetric Synthesis:
(1R,2R)-N,N-dimethylcyclopentane-1,2-diamine is applied in asymmetric synthesis to create enantiomerically pure compounds, which are important in pharmaceuticals and other industries where the stereochemistry of molecules affects their properties and activities.
Used in Medicinal Chemistry:
Its unique structure and chirality make (1R,2R)-N,N-dimethylcyclopentane-1,2-diamine a valuable component in medicinal chemistry, where it can be used in the design and synthesis of new pharmaceuticals with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 942492-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,2,4,9 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.Calculate Digit Verification of CAS Registry Number 942492-63:
(8*9)+(7*4)+(6*2)+(5*4)+(4*9)+(3*2)+(2*6)+(1*3)=189
189 % 10 = 9
So 942492-63-9 is a valid CAS Registry Number.
942492-63-9Upstream product
942492-63-9Downstream Products
- 1095647-94-1 C19H24F3N5O2S
- 1095647-96-3 C19H25F3N6O2S
- 1095647-97-4 C23H31F3N6O
- 1095647-98-5 C21H27F3N6O
- 1173911-10-8 C21H29F3N6OS
- 1173911-16-4 C21H29F3N6OS
- 1173911-08-4 C21H29F3N6OS
- 1173911-15-3 C20H27F3N6OS
- 1173911-07-3 C20H27F3N6OS
- 1173911-01-7 C22H31F3N6OS
- 1173911-00-6 C21H29F3N6OS
- 1173910-99-0 C20H27F3N6OS
- 1058130-49-6 8-cyclohexyl-N1a-((1R,2R)-2-(dimethylamino)cyclopentyl)-N5-((dimethylamino)sulfonyl)-11-methoxy-1,12b-dihydrocyclopropa[d]indolo[2,1-a][2]benzazepine-1a,5(2H)-dicarboxamide
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(1R,2R)-N,N-dimethylcyclopentane-1,2-diamine
