105931-57-5 | N4-Benzoyl-2'-deoxy-5'-O-DMT-5-methylcytidine 3'-CE phosphoramidite

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$36.00	$25.00
1g	95%	in stock	$93.00	$65.00
5g	95%	in stock	$328.00	$229.00
25g	95%	in stock	$1,145.00	$801.00

Description

• Catalog Number: AE10210
• Chemical Name: N4-Benzoyl-2'-deoxy-5'-O-DMT-5-methylcytidine 3'-CE phosphoramidite
• CAS Number: 105931-57-5
• Molecular Formula: C47H54N5O8P
• Molecular Weight: 847.9341
• MDL Number: MFCD00148939
• SMILES: N#CCCOP(N(C(C)C)C(C)C)O[C@H]1C[C@@H](O[C@@H]1COC(c1ccc(cc1)OC)(c1ccc(cc1)OC)c1ccccc1)n1cc(C)c(nc1=O)NC(=O)c1ccccc1

Computed Properties

• Complexity: 1490
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 3
• Heavy Atom Count: 61
• Hydrogen Bond Acceptor Count: 10
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 19
• Undefined Atom Stereocenter Count: 1
• XLogP3: 7.2

Upstream Synthesis Route

Cytidine, N-benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxy-5-methyl-, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite] is a key reagent used in chemical synthesis processes, particularly in the field of nucleoside modification. This compound serves as a versatile building block that allows for the selective and controlled modification of nucleosides, which are essential components in DNA and RNA synthesis. By utilizing this phosphoramidite derivative, researchers can introduce specific functional groups or structural modifications at precise positions within nucleoside sequences, enabling the design and synthesis of custom nucleic acid analogs with desired properties and characteristics. This advanced reagent plays a crucial role in the synthesis of modified nucleosides for various applications in drug development, molecular biology, and other research areas that require tailored nucleic acid structures.