2'-OMe-iBu-G Phosphoramidite - for DNA synthesis, Suitable for molecular biology, ≥98% , CAS No.150780-67-9

CAS: 150780-67-9 Cat. No.: M776846 Formula: C₄₅H₅₆N₇O₉P Peso molecolare: 869.94 Numero EC: 892-126-5

GRADE & PURITY Suitable for molecular biology, for DNA synthesis, ≥98%

Synonyms

2'-OMe-ibu-G Phosphoramidite | 2'-OMe-G(ibu) Phosphoramidite | 2'-OMe-G(iBu)-3'-phosphoramidite | (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-methoxytetrahydrofuran-3-yl (2-cyanoethyl

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Panoramica

2'-OMe-G(ibu) Phosphoramidite is a modified phosphoramidite monomer, which can be used for the synthesis of oligonucleotides.

Specifications

Sinonimi

2'-OMe-ibu-G Phosphoramidite | 2'-OMe-G(ibu) Phosphoramidite | 2'-OMe-G(iBu)-3'-phosphoramidite | (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-methoxytetrahydrofuran-3-yl (2-cyanoethyl

Specifiche e purezza

for DNA synthesis, Suitable for molecular biology, ≥98%

Condizioni di conservazione di stoccaggio

Protected from light,Store at -20°C,Argon charged

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

for DNA synthesis, Suitable for molecular biology

Tipo di azione

ACTIVATOR

Purezza

≥98%

Nomi e identificatori

• Sorrisi canonici: CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)OP(N(C(C)C)C(C)C)OCCC#N)OC
• IUPAC Name: N-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide
• InChIKey: IRRDHRZUOZNWDJ-MLLDKZSOSA-N
• INCHI: 1S/C45H56N7O9P/c1-28(2)41(53)49-44-48-40-37(42(54)50-44)47-27-51(40)43-39(57-9)38(61-62(59-25-13-24-46)52(29(3)4)30(5)6)36(60-43)26-58-45(31-14-11-10-12-15-31,32-16-20-34(55-7)21-17-32)33-18-22-35(56-8)23-19-33/h10-12,14-23,27-30,36,38-39,43H,13,25-26H2,1-9H3,(H2,48,49,50,53,54)/t36-,38-,39-,43-,62?/m1/s1
• Isomeri SMILES: CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)OP(N(C(C)C)C(C)C)OCCC#N)OC
• Peso molecolare: 869.94

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Triphenyl compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Triphenyl compounds
• Alternative Parents: Ribonucleoside phosphoramidites Glycosylamines 6-oxopurines Hypoxanthines Benzylethers Phenoxy compounds Anisoles N-arylamides Methoxybenzenes Alkyl aryl ethers Pyrimidones N-substituted imidazoles Monosaccharides Vinylogous amides Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides Dialkyl ethers Oxacyclic compounds Azacyclic compounds Nitriles Organic oxides Carbonyl compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Triphenyl compound - Ribonucleoside phosphoramidite - N-glycosyl compound - Glycosyl compound - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - Benzylether - Phenol ether - Phenoxy compound - N-arylamide - Anisole - Methoxybenzene - Pyrimidone - Alkyl aryl ether - Pyrimidine - Monosaccharide - Monocyclic benzene moiety - N-substituted imidazole - Azole - Heteroaromatic compound - Oxolane - Vinylogous amide - Imidazole - Secondary carboxylic acid amide - Carboxamide group - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Nitrile - Carbonitrile - Organic oxygen compound - Cyanide - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Sensibilità: Moisture & heat sensitive