1312611-48-5
Post Buying Request-
-
Basic information
- Product Name: 2-(2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1H-imidazol-4-yl)naphthalen-6-yl trifluoromethanesulfonate
- Synonyms: 2-(2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1H-imidazol-4-yl)naphthalen-6-yl trifluoromethanesulfonate
- CAS NO:1312611-48-5
- Molecular Formula:
- Molecular Weight: 0
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1312611-48-5.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-(2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1H-imidazol-4-yl)naphthalen-6-yl trifluoromethanesulfonate(CAS DataBase Reference)
- NIST Chemistry Reference: 2-(2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1H-imidazol-4-yl)naphthalen-6-yl trifluoromethanesulfonate(1312611-48-5)
- EPA Substance Registry System: 2-(2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1H-imidazol-4-yl)naphthalen-6-yl trifluoromethanesulfonate(1312611-48-5)
-
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: 1312611-48-5(Hazardous Substances Data)
1312611-48-5 Suppliers
Recommended suppliersmore
1312611-48-5 Usage
Naphthalene moiety
A fused two-ring structure consisting of two benzene rings, contributing to the compound's stability and aromaticity.Imidazole ring
A five-membered ring with one nitrogen atom and four carbon atoms, providing a basic nitrogen environment and potential coordination sites for metal ions.Trifluoromethanesulfonate group
A highly electron-withdrawing group (-CF3SO3) that imparts acidity and reactivity to the compound, making it a good leaving group in substitution reactions.Tert-butoxycarbonyl (Boc) protecting group
A bulky, electron-withdrawing group (-OC(CH3)3) that protects the pyrrolidine nitrogen from unwanted reactions, allowing for selective activation and deprotection steps in synthetic routes.Stereochemistry
The presence of the (S)-configuration at the 1-position of the pyrrolidine ring introduces chirality to the molecule, which may be important for its biological activity and selectivity.Potential applications
Due to its diverse structure and reactivity, this compound may be used in organic synthesis, chemical reactions, and as a building block for the synthesis of more complex molecules, including pharmaceuticals.Check Digit Verification of cas no
The CAS Registry Mumber 1312611-48-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,6,1 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.Calculate Digit Verification of CAS Registry Number 1312611-48:
(9*1)+(8*3)+(7*1)+(6*2)+(5*6)+(4*1)+(3*1)+(2*4)+(1*8)=105
105 % 10 = 5
So 1312611-48-5 is a valid CAS Registry Number.
1312611-48-5Upstream product
1312611-48-5Downstream Products
Post a RFQ
1
What can I do for you?
Get Best Price
Get Best Price for 1312611-48-5
2-(2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1H-imidazol-4-yl)naphthalen-6-yl trifluoromethanesulfonate
