5-Nitrothiazole - ≥98% , CAS No.14527-46-9

CAS: 14527-46-9 Cat. No.: N181541 Molecular Weight: 130.1
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
5-Nitro-1,3-thiazole # | SCHEMBL375485 | A3156 | 5-nitrothiazole | FT-0645821 | MFCD08436042 | 5-Nitro-1,3-thiazole | DTXSID70337299 | Thiazole, 5-nitro- | Thiazole,5-nitro- | BL006203 | AKOS005146119 | AS-45763 | VVVCJCRUFSIVHI-UHFFFAOYSA-N | Nandrolonep
Storage
Protected from light,Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250mg
N181541-250mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$39.90
1g
N181541-1g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$89.90
5g
N181541-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$279.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
5-Nitro-1, 3-thiazole # | SCHEMBL375485 | A3156 | 5-nitrothiazole | FT-0645821 | MFCD08436042 | 5-Nitro-1, 3-thiazole | DTXSID70337299 | Thiazole, 5-nitro- | Thiazole, 5-nitro- | BL006203 | AKOS005146119 | AS-45763 | VVVCJCRUFSIVHI-UHFFFAOYSA-N | Nandrolonep
Specifications & Purity
≥98%
Storage
Protected from light, Room temperature, Argon charged
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Canonical SmilesC1=C(SC=N1)[N+](=O)[O-]
IUPAC Name5-nitro-1,3-thiazole
InChIKeyVVVCJCRUFSIVHI-UHFFFAOYSA-N
INCHI1S/C3H2N2O2S/c6-5(7)3-1-4-2-8-3/h1-2H
Isomeric SMILES C1=C(SC=N1)[N+](=O)[O-]
Molecular Weight 130.1
Reaxy-Rn 116971
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=116971&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassAzoles
SubclassThiazoles
Intermediate Tree Nodes Not available
Direct ParentNitrothiazoles
Alternative Parents Nitroaromatic compounds  Heteroaromatic compounds  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Nitroaromatic compound - Nitrothiazole - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Azacycle - Organic 1,3-dipolar compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic zwitterion - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitrothiazoles. These are compounds containing a thiazole ring which bears a nitro group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(non-human)
Leishmania amazonensis (3813 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania mexicana (936 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichomonas vaginalis (2376 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Giardia intestinalis (1290 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Molecular Weight130.130 g/mol
XLogP31.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass129.984 Da
Monoisotopic Mass129.984 Da
Topological Polar Surface Area87.000 Ų
Heavy Atom Count8
Formal Charge0
Complexity102.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Haoyu Long, Yanhao Jiang, Yanjuan Liu, Yuefei Zhang, Wei Chen, Sheng Tang.  (2023)  Chromatographic separation performance of silica microspheres surface-modified with triazine-containing imine-linked covalent organic frameworks.  TALANTA,      [PMID:37126925] [10.1016/j.talanta.2023.124589]
2. Zhefei Hu, Yanhao Jiang, Panpan Cao, Yanjuan Liu, Yuefei Zhang, Wei Chen, Sheng Tang.  (2023)  Performance evaluation of 2-undecylimidazole/propyl methacrylate bifunctional silica gel for mixed-mode reversed-phase/anion-exchange chromatography.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2023.108768]
Solution Calculators
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