15410-48-7 Usage
Molecular weight
384.36 g/mol
Functional groups
Acetate (COCH3), Methylsulfonyl (SO2CH3), Hydroxyl (OH)
Structure
A derivative of D-mannitol with two methylsulfonyl groups at the 1 and 6 positions and four acetate groups at the 2, 3, 4, and 5 positions.
Use as a protecting group
1-O,6-O-Bis(methylsulfonyl)-D-mannitol 2,3,4,5-tetraacetate is commonly used in organic synthesis as a protecting group for hydroxyl groups.
Versatility
The presence of multiple functional groups makes it suitable for chemical modification and manipulation.
Stability
1-O,6-O-Bis(methylsulfonyl)-D-mannitol 2,3,4,5-tetraacetate is stable and resistant to many reaction conditions, making it useful in the synthesis of complex organic molecules and pharmaceuticals.
Role in research
Due to its stability and versatility, 1-O,6-O-Bis(methylsulfonyl)-D-mannitol 2,3,4,5-tetraacetate plays a crucial role in the development of new drugs and materials in medicinal and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 15410-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,1 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15410-48:
(7*1)+(6*5)+(5*4)+(4*1)+(3*0)+(2*4)+(1*8)=77
77 % 10 = 7
So 15410-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H26O14S2/c1-9(17)27-13(7-25-31(5,21)22)15(29-11(3)19)16(30-12(4)20)14(28-10(2)18)8-26-32(6,23)24/h13-16H,7-8H2,1-6H3
