127556-03-0 Usage
Description
(2R)-BORNANE-10,2-SULTAM GLYCINATE is a chemical compound with a molecular formula of C10H18N2O7S and a molecular weight of 302.32 g/mol. It is a white crystalline powder that is soluble in water and has a melting point of 206-208°C. The (2R)-configuration of the compound indicates that it has a specific arrangement of atoms in its structure, which can affect its properties and reactivity. Overall, (2R)-bornane-10,2-sultam glycinate is a versatile compound with various applications in the chemical and pharmaceutical industries.
Uses
Used in Pharmaceutical Industry:
(2R)-BORNANE-10,2-SULTAM GLYCINATE is used as an intermediate in the synthesis of various medications for its specific arrangement of atoms and reactivity.
Used in Production of Fine Chemicals and Polymers:
(2R)-BORNANE-10,2-SULTAM GLYCINATE is used as a key component in the production of fine chemicals and polymers due to its unique properties and solubility in water.
Check Digit Verification of cas no
The CAS Registry Mumber 127556-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,5 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127556-03:
(8*1)+(7*2)+(6*7)+(5*5)+(4*5)+(3*6)+(2*0)+(1*3)=130
130 % 10 = 0
So 127556-03-0 is a valid CAS Registry Number.
127556-03-0Relevant articles and documents
Stereocontrolled 1,3-dipolar cycloadditions using Oppolzer's camphor sultam as the chiral auxiliary for carbonyl stabilized azomethine ylides
Garner, Philip,Dogan, ?zdemir,Youngs, Wiley J.,Kennedy, Vance O.,Protasiewicz, John,Zaniewski, Rebecca
, p. 71 - 85 (2007/10/03)
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddition reactions of chiral azomethine ylides are described. In one approach, chiral azomethine ylides were generated by thermolysis of aziridine carboxylate sultams and trapped with a variety of dipolarophiles to give good yields of the corresponding cycloadducts. In the second approach, chiral azomethine ylides were generated from glycyl sultams by 'imine tautomerization' and trapped with dipolarophiles to give good yields of the corresponding cycloadducts.
