N-(4-(N-(Thiazol-2-yl)sulfamoyl)phenyl)acetamide - ≥95% , CAS No.127-76-4

CAS: 127-76-4 Cat. No.: N694180 Molecular Weight: 297.4 EC Number: 204-864-1
AVAILABLE TO ORDER
GRADE & PURITY ≥95%
Storage
Protected from light,Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
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Status
Price
Qty
100mg
N694180-100mg
2

$51.90

$77.90
Save $26.00 (33.38%)
250mg
N694180-250mg
1

$100.90

$151.90
Save $51.00 (33.57%)
1g
N694180-1g
1

$245.90

$368.90
Save $123.00 (33.34%)
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Why this grade

≥95% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Specifications & Purity
≥95%
Storage
Protected from light, Room temperature, Argon charged
Shipped In
Normal
Purity
≥95%
Names and Identifiers
Canonical SmilesCC(=O)NC1=CC=C(C=C1)S(=O)(=O)NC2=NC=CS2
IUPAC NameN-[4-(1,3-thiazol-2-ylsulfamoyl)phenyl]acetamide
InChIKeyKXNXWINFSDKMHD-UHFFFAOYSA-N
INCHI1S/C11H11N3O3S2/c1-8(15)13-9-2-4-10(5-3-9)19(16,17)14-11-12-6-7-18-11/h2-7H,1H3,(H,12,14)(H,13,15)
Isomeric SMILES CC(=O)NC1=CC=C(C=C1)S(=O)(=O)NC2=NC=CS2
Alternate CAS 127-76-4
Molecular Weight 297.4
Reaxy-Rn 287921
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=287921&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
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzenesulfonamides
Intermediate Tree Nodes Not available
Direct ParentBenzenesulfonamides
Alternative Parents Acetanilides  N-acetylarylamines  Benzenesulfonyl compounds  Organosulfonamides  Thiazoles  Heteroaromatic compounds  Aminosulfonyl compounds  Acetamides  Secondary carboxylic acid amides  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Acetanilide - Benzenesulfonamide - N-acetylarylamine - Benzenesulfonyl group - Anilide - N-arylamide - Organosulfonic acid amide - Azole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiazole - Aminosulfonyl compound - Acetamide - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Organic oxygen compound - Organopnictogen compound - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
External Descriptors sulfonamide - 1,3-thiazole - acetamides
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NS1 Nonstructural protein 1 (33327 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:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeDateItem
J2528478Certificate of AnalysisAug 27, 2025 N694180
J2528479Certificate of AnalysisAug 27, 2025 N694180
J2528480Certificate of AnalysisAug 27, 2025 N694180
Chemical and Physical Properties
Molecular Weight297.400 g/mol
XLogP3-0.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count4
Exact Mass297.024 Da
Monoisotopic Mass297.024 Da
Topological Polar Surface Area125.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity413.000
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. Chao Liang, Jingyang Zhao, Pingdong Wei, Kang Wei, Hanqing Jiang.  (2025)  An energy-embodied paralleled liquid manipulation for equipment-free, quantitative multiplexed liver function monitoring.  Science Advances,  11  (32):   [PMID:40779627] [10.1126/sciadv.adx0092]
Solution Calculators
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