2-Aminothiazole - ≥97% , CAS No.96-50-4

Name: 2-Aminothiazole - ≥97% , CAS No.96-50-4
SKU: A104872
Availability: InStock

CAS: 96-50-4 Cat. No.: A104872 Formula: C₃H₄N₂S Molecular Weight: 100.14 Beilstein Registry Number: 105738 EC Number: 202-511-6

10 Citations COA

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2-Aminothiazole - ≥97% CAS No(96-50-4) by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY ≥97%

Synonyms

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product Solution Calculators Reviews

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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

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

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Quality documents

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

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Literature proof

Cited in 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Usually used in the synthesis of 2-aminothiazole-modified silica gel，and aslo used in Ulmann coupling with 2-chlorobenzoic acids mediated by ultrasonic irradiation.

Specifications

Synonyms

Specifications & Purity

≥97%

Biochemical and Physiological Mechanisms

2-Aminothiazole is a potent cyclin-dependent kinase 5 inhibitor and is a therapeutic drug for Alzheimer's disease and other neurodegenerative diseases.

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Purity

≥97%

Names and Identifiers

Pubchem Sid

488179668

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488179668

Canonical Smiles

C1=CSC(=N1)N

IUPAC Name

1,3-thiazol-2-amine

InChIKey

RAIPHJJURHTUIC-UHFFFAOYSA-N

INCHI

1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)

Isomeric SMILES

C1=CSC(=N1)N

WGK Germany

RTECS

XJ2100000

Alternate CAS

6142-05-8

Molecular Weight

100.14

Beilstein

105738

Reaxy-Rn

105738

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=105738&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.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Azoles
    - Subclass Thiazoles

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Azoles
Subclass	Thiazoles
Intermediate Tree Nodes	Not available
Direct Parent	Thiazoles
Alternative Parents	Heteroaromatic compounds Isothioureas Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Heteroaromatic compound - Thiazole - Isothiourea - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as thiazoles. These are heterocyclic compounds containing a five-member aromatic ring made up of one sulfur atom, one nitrogen, and three carbon atoms.
External Descriptors	1,3-thiazole - primary amino compound
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

3D Structure

Associated Targets(Human)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOA Tclin Monoamine oxidase A (11911 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOB Tclin Monoamine oxidase B (8835 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PRKAA2 Tchem AMP-activated protein kinase, alpha-2 subunit (1328 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NOS1 Tchem Nitric-oxide synthase, brain (1786 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

Discover Target: HSD17B10

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

Discover Target: SLCO1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GLS Tchem Glutaminase kidney isoform, mitochondrial (16997 Activities)

Discover Target: GLS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

ddlB D-alanylalanine synthetase (66 Activities)

Discover Target: ddlB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

murA UDP-N-acetylglucosamine 1-carboxyvinyltransferase (389 Activities)

Discover Target: murA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nos2 Nitric oxide synthase, inducible (3573 Activities)

Discover Target: Nos2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Salmonella typhimurium (15756 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasmodium falciparum (966862 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cavia porcellus (23802 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasma (328 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay 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.

26 results found

Lot Number	Certificate Type	Date	Item
J2220106	Certificate of Analysis	Jul 30, 2026	A104872
J2220103	Certificate of Analysis	Jul 30, 2026	A104872
J2220094	Certificate of Analysis	Jul 30, 2026	A104872
J2220093	Certificate of Analysis	Jul 30, 2026	A104872
H2201067	Certificate of Analysis	May 11, 2026	A104872
A2613251	Certificate of Analysis	Dec 16, 2025	A104872
L2519121	Certificate of Analysis	Dec 16, 2025	A104872
A2613264	Certificate of Analysis	Dec 16, 2025	A104872
C1802027	Certificate of Analysis	Oct 14, 2025	A104872
A2604140	Certificate of Analysis	Nov 05, 2024	A104872
K2420099	Certificate of Analysis	Nov 05, 2024	A104872
K2412247	Certificate of Analysis	Nov 05, 2024	A104872
K2412164	Certificate of Analysis	Nov 05, 2024	A104872
K2412158	Certificate of Analysis	Nov 05, 2024	A104872
K2412148	Certificate of Analysis	Nov 05, 2024	A104872
D2013124	Certificate of Analysis	Jan 30, 2024	A104872
G1527002	Certificate of Analysis	Mar 08, 2023	A104872
B2322249	Certificate of Analysis	Feb 25, 2023	A104872
H2318186	Certificate of Analysis	Feb 15, 2023	A104872
H2318184	Certificate of Analysis	Feb 15, 2023	A104872
H2318183	Certificate of Analysis	Feb 15, 2023	A104872
H2318182	Certificate of Analysis	Feb 15, 2023	A104872
I1827030	Certificate of Analysis	Aug 06, 2022	A104872
B2322295	Certificate of Analysis	Jul 26, 2022	A104872
F2223102	Certificate of Analysis	Jun 25, 2022	A104872
F2222470	Certificate of Analysis	Jun 25, 2022	A104872

Chemical and Physical Properties

Solubility	Soluble in water, alcohol and ether
Sensitivity	Light Sensitive,Air Sensitive
Boil Point(°C)	117°C
Melt Point(°C)	93°C
Molecular Weight	100.140 g/mol
XLogP3	0.400
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	0
Exact Mass	100.01 Da
Monoisotopic Mass	100.01 Da
Topological Polar Surface Area	67.200 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	48.100
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Documents & Articles

1,3-Thiazole building blocks in natural products and synthetic materials

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

1,3-Thiazole building blocks

A Comprehensive Overview of Thiazole: Structural Features, Application Value, Selection Considerations, and Product Navigation (Tables 1–4)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

heterocyclic chemistry Thiazole azole

Direct Construction of Methylsulfonyl-Containing Heterocycles: Synthesis and Applications of Prefunctionalized Three-Carbon Vinamidinium Salts

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

–SO₂CH₃ –SO₂Me

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📚 Citations by Application

Extraction & workup solvent4

Organic synthesis — reaction medium9

Crystallization & recrystallization1

Electrochemistry & battery electrolyte3

Industrial & non-pharma application2

Other applications2

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2-Aminothiazole - 10mM in DMSO , CAS No.96-50-4

2-Aminothiazole - ≥97% , CAS No.96-50-4

Storage & shipping

Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Customer Reviews

📚 Citations by Application

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