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BX LAB PRODUCT CATEGORY

Base-protected Nucleosides

Quick view. Nucleosides bearing base-protecting groups for controlled phosphorylation, phosphitylation and oligonucleotide synthesis. This category currently includes 36 products. Base-protected Nucleosides products serve as starting materials, protected intermediates and analytical comparators in nucleoside, nucleotide and oligonucleotide chemistry.

Products36
Use scopeResearch use only
Pack sizeCustomized to requirements
SupportSelection and custom synthesis review

Category guide

Typical use

Base-protected Nucleosides products serve as starting materials, protected intermediates and analytical comparators in nucleoside, nucleotide and oligonucleotide chemistry.

How to select

Confirm anomeric and sugar stereochemistry, base identity, substitution position, protecting-group pattern and required downstream transformation.

How to qualify

Use orthogonal identity data such as NMR and MS together with chromatographic purity, water or residual-solvent review and route-specific impurity controls.

Product-family considerations

Common advantages
  • Nucleoside catalogs provide flexible entry points for protecting-group, phosphorylation and glycosylation-route development.
  • Availability of related analogs helps researchers compare base, sugar and substitution effects systematically.
Common limitations
  • Downstream use often requires additional protection, activation or purification before incorporation into oligonucleotide workflows.
  • Isomeric purity, water content and residual solvents should be matched to the planned chemistry.

Category literature

These publications provide background for the Base-protected Nucleosides product family. Individual product pages only show additional product- or feature-relevant references.

Selection checklist

Exact identityMatch the canonical name with a CAS number, structure, SMILES or drawing; confirm stereochemistry, protecting groups and salt form where applicable.
SpecificationDefine target purity, analytical method, water or residual-solvent concerns and any application-specific acceptance limits.
Workflow fitShare the reaction, enzyme, sequence, solvent system, support or analytical method used to evaluate compatibility.
Supply needProvide initial quantity, expected future scale, packaging preference, timeline and documentation requirements.

36 products

Chemical structure of 2',3'-dideoxy-C(Ac)2',3'-dideoxy-C(Ac)

≥98% · CAS: 119818-52-9

BX-PN-0002
Structure of BX-PN-00872'-O-propargyl-rC(Bz)

≥98% · CAS: 210096-41-6

BX-PN-0087
Chemical structure of N6-benzoyl-2'-O-methyladenosineN6-Benzoyl-2'-O-methyladenosine

≥98% · CAS: 85079-00-1

BX-PN-0107
Structure of N6-benzoyl-2'-fluoro-2'-deoxyadenosine2'-F-dA(Bz)

≥98% · CAS: 136834-20-3

BX-PN-0096
Structure of N2-isobutyrylguanosinerG(iBu)

≥98% · CAS: 64350-24-9

BX-PN-0102
Structure of N4-benzoyl-2'-deoxycytidine2'-dC(Bz)

≥98% · CAS: 4836-13-9

BX-PN-0105
Chemical structure of N2-isobutyryl-2'-fluoro-2'-deoxyguanosineN2-Isobutyryl-2'-fluoro-2'-deoxyguanosine

≥98% · CAS: 80681-25-0

BX-PN-0110
Chemical structure of 2',3'-dideoxy-C(Bz)2',3'-dideoxy-C(Bz)

≥98% · CAS: 120885-60-1

BX-PN-0003
Structure of N4-benzoyl-2'-O-MOE-5-methylcytidine2'-O-MOE-5-Me-rC(Bz)

≥98% · CAS: 340162-93-8

BX-PN-0080
Structure of N6-benzoyl-2'-O-MOE adenosine2'-O-MOE-rA(Bz)

≥98% · CAS: 333335-93-6

BX-PN-0082
Structure of N4-acetylcytidinerC(Ac)

≥98% · CAS: 3768-18-1

BX-PN-0091
Structure of N4-acetyl-2'-deoxycytidine2'-dC(Ac)

≥98% · CAS: 32909-05-0

BX-PN-0092
Structure of N4-acetyl-2'-fluoro-2'-deoxycytidine2'-F-dC(Ac)

≥98% · CAS: 159414-97-8

BX-PN-0097
Structure of N4-acetyl-2'-O-methylcytidine2'-O-Me-rC(Ac)

≥98% · CAS: 113886-71-8

BX-PN-0100
Structure of N4-benzoyl-2'-O-methylcytidine2'-O-Me-rC(Bz)

≥98% · CAS: 52571-45-6

BX-PN-0101
Structure of N6-benzoyladenosinerA(Bz)

≥98% · CAS: 4546-55-8

BX-PN-0103
Structure of N4-benzoylcytidinerC(Bz)

≥98% · CAS: 13089-48-0

BX-PN-0104
Chemical structure of N6-benzoyl-2'-deoxyadenosineN6-Benzoyl-2'-deoxyadenosine

≥98% · CAS: 4546-72-9

BX-PN-0106
Chemical structure of N2-isobutyryl-2'-deoxyguanosineN2-Isobutyryl-2'-deoxyguanosine

≥98% · CAS: 68892-42-2

BX-PN-0109
Chemical structure of 2'-Deoxy-O6-[2-(4-nitrophenylethyl)]guanosine2'-Deoxy-O6-[2-(4-nitrophenylethyl)]guanosine

≥98% · CAS: 86137-72-6

BX-MN-0701
Structure of N2-dimethylformamidine-2'-fluoro-2'-deoxyguanosine2'-F-dG(DMF)

≥98% · CAS: N/A

BX-PN-0005
Structure of N4-benzoyl-5-methyl-2'-O,4'-C-methylenecytidine2'-O-4'-C-Locked-5-Me-rC(Bz)

≥98% · CAS: 206055-81-4

BX-PN-0006
Structure of N4-benzoyl-2'-O,4'-C-methylenecytidine2'-O-4'-C-Locked-rC(Bz)

≥98% · CAS: 221229-74-9

BX-PN-0007
Structure of N2-isobutyryl-2'-O,4'-C-methyleneguanosine2'-O-4'-C-Locked-rG(iBu)

≥98% · CAS: 206055-68-7

BX-PN-0009
Structure of N4-benzoyl-3'-O-carbamoyl-2'-deoxycytidine3'-O-carbamoyl-2'-dC(Bz)

≥98% · CAS: N/A

BX-PN-0021
Structure of N4-benzoyl deoxycytidine analogue with a 3'-carboxamide3'-amide-2'-dC(Bz)

≥98% · CAS: N/A

BX-PN-0022
Structure of N4-benzoyl deoxycytidine analogue with a 3'-ureido substituent3'-ureido-2'-dC(Bz)

≥98% · CAS: N/A

BX-PN-0023
Structure of N6-benzoyl-3'-O-methyladenosine3'-O-Me-rA(Bz)

≥98% · CAS: 85090-30-8

BX-PN-0074
Structure of N4-benzoyl-2'-O-MOE cytidine2'-O-MOE-rC(Bz)

≥98% · CAS: 2305416-18-4

BX-PN-0083
Structure of N4-acetyl-2'-O-MOE cytidine2'-O-MOE-rC(Ac)

≥98% · CAS: 2049081-09-4

BX-PN-0084
Structure of N2-isobutyryl-2'-O-propargylguanosine2'-O-propargyl-rG(iBu)

≥98% · CAS: 2095417-55-1

BX-PN-0085
Structure of N6-benzoyl-2'-O-propargyladenosine2'-O-propargyl-rA(Bz)

≥98% · CAS: 210096-44-9

BX-PN-0086
Structure of N4-acetyl-2'-O-propargylcytidine2'-O-propargyl-rC(Ac)

≥98% · CAS: 1498305-49-9

BX-PN-0088
Structure of N6-benzoyl-2'-O,4'-C-methyleneadenosine2'-O-4'-C-Locked-rA(Bz)

≥98% · CAS: 209968-94-5

BX-PN-0090
Structure of N4-benzoyl-2'-fluoro-2'-deoxycytidine2'-F-dC(Bz)

≥98% · CAS: 146954-76-9

BX-PN-0098
Structure of N2-isobutyryl-2'-O-methylguanosine2'-O-Me-rG(iBu)

≥98% · CAS: 63264-29-9

BX-PN-0099

Frequently asked questions

What are typical uses for Base-protected Nucleosides?

Base-protected Nucleosides products serve as starting materials, protected intermediates and analytical comparators in nucleoside, nucleotide and oligonucleotide chemistry.

What should be confirmed before ordering Base-protected Nucleosides?

Confirm anomeric and sugar stereochemistry, base identity, substitution position, protecting-group pattern and required downstream transformation.

Are custom quantities or related analogs available?

BX Lab reviews custom package sizes, catalog-adjacent analogs and research-use custom synthesis requests against the target structure, purity, scale and timeline.

Need help selecting a product?

Tell our scientists about your target chemistry, workflow, required purity and scale. We can help identify a catalog product, related analog or custom route.

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