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STA Pharmaceutical DNA 5-(E)-acrylamide-C6-amine(TFA)-U amidite | 200 mg | CAS 178925-21-8 | MDL MFCD08061991

Catalog No. 502363858
Encompass

DNA 5-(E)-acrylamide-C6-amine(TFA)-U amidite is a Amidite reagent (Subcategory: Uracil Series) sold by WuXi TIDES. Offered in 200 mg. Store at -20 °C. SDS available for reference.

Specifications
- CAS: 178925-21-8
- MDL: MFCD08061991
- InChIKey: XHGOWDJUVKONLU-HAKODNTASA-N
- Molecular Weight: 995.046971487
- Molecular Formula: C50H62F3N6O10P
- Purity: ≥95%
- Container Type: 15 mL HDPE
- Pack Size: 200 mg
- Net Weight: 0.2 g
- Gross Weight: 6.9 g
- Commodity Code: 29349990
- Country Of Origin: China
- IUPAC: (2R,3S,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-5-((E)-3-oxo-3-((6-(2,2,2-trifluoroacetamido)hexyl)amino)prop-1-en-1-yl)-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
- SMILES: O=C(C(/C=C/C(NCCCCCCNC(C(F)(F)F)=O)=O)=CN1[C@H]2C[C@@H]([C@H](O2)COC(C3=CC=C(C=C3)OC)(C4=CC=C(C=C4)OC)C5=CC=CC=C5)OP(OCCC#N)N(C(C)C)C(C)C)NC1=O

Catalog No. 50-236-3858 Supplier STA Pharmaceutical Supplier No. STAAM10537200MG
May include imposed supplier surcharges.
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DNA 5-(E)-acrylamide-C6-amine(TFA)-U amidite is a Amidite reagent (Subcategory: Uracil Series) sold by WuXi TIDES. Offered in 200 mg. Store at -20 °C. SDS available for reference.

Specifications
- CAS: 178925-21-8
- MDL: MFCD08061991
- InChIKey: XHGOWDJUVKONLU-HAKODNTASA-N
- Molecular Weight: 995.046971487
- Molecular Formula: C50H62F3N6O10P
- Purity: ≥95%
- Container Type: 15 mL HDPE
- Pack Size: 200 mg
- Net Weight: 0.2 g
- Gross Weight: 6.9 g
- Commodity Code: 29349990
- Country Of Origin: China
- IUPAC: (2R,3S,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-5-((E)-3-oxo-3-((6-(2,2,2-trifluoroacetamido)hexyl)amino)prop-1-en-1-yl)-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
- SMILES: O=C(C(/C=C/C(NCCCCCCNC(C(F)(F)F)=O)=O)=CN1[C@H]2C[C@@H]([C@H](O2)COC(C3=CC=C(C=C3)OC)(C4=CC=C(C=C4)OC)C5=CC=CC=C5)OP(OCCC#N)N(C(C)C)C(C)C)NC1=O

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