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

CAS: 96-50-4 Cat. No.: A427168 Peso molecular: 100.14 Beilstein Registry Number: 105738 Número EC: 202-511-6
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
2-Amino-1,3-thiazole | AKOS000119189 | Aminothiazol | CHEBI:40782 | Thiazol-2-ylamine | thiazol-2-yl-amine | thiazolyl amine | 2-imino-2,3-dihydro-1,3-thiazole | DivK1c_000176 | KBio2_000505 | thiazol-2-amine | HY-12396 | SCHEMBL7401 | 2-amino-1,3 thiazol
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
A427168-1ml
2

58,90US$

69,90US$
Guardar 11,00 US$ (15.74%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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.

📚

Literature proof

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

Descripción general

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

Sinónimos
2-Amino-1, 3-thiazole | AKOS000119189 | Aminothiazol | CHEBI:40782 | Thiazol-2-ylamine | thiazol-2-yl-amine | thiazolyl amine | 2-imino-2, 3-dihydro-1, 3-thiazole | DivK1c_000176 | KBio2_000505 | thiazol-2-amine | HY-12396 | SCHEMBL7401 | 2-amino-1, 3 thiazol
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
2-Aminothiazole is a potent cyclin-dependent kinase 5 inhibitor and is a therapeutic drug for Alzheimer's disease and other neurodegenerative diseases.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Nombres e identificadores
Sonrisas canónicasC1=CSC(=N1)N
IUPAC Name1,3-thiazol-2-amine
InChIKeyRAIPHJJURHTUIC-UHFFFAOYSA-N
INCHI1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)
Isómeros SMILES C1=CSC(=N1)N
WGK Alemania 3
RTECS XJ2100000
CAS alternativo 6142-05-8
Peso molecular 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.

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
ClaseAzoles
SubclassThiazoles
Intermediate Tree Nodes Not available
Direct ParentThiazoles
Alternative Parents Heteroaromatic compounds  Isothioureas  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Heteroaromatic compound - Thiazole - Isothiourea - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRKAA2 Tchem AMP-activated protein kinase, alpha-2 subunit (1328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NOS1 Tchem Nitric-oxide synthase, brain (1786 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLS Tchem Glutaminase kidney isoform, mitochondrial (16997 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
ddlB D-alanylalanine synthetase (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
murA UDP-N-acetylglucosamine 1-carboxyvinyltransferase (389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Salmonella typhimurium (15756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cavia porcellus (23802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadLight sensitive.
Punto de ebullición (°C)117°C
Punto de fusión (°C)93°C
Peso molecular100.140 g/mol
XLogP30.400
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass100.01 Da
Monoisotopic Mass100.01 Da
Topological Polar Surface Area67.200 Ų
Heavy Atom Count6
Formal Charge0
Complexity48.100
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Pei Chen, Hui Zhu, Tianhao Na, Yong Yi, Jian Zhou, Tao Duan, Jiehong Lei.  (2023)  Functionalized collagen fiber with specific recognition sites for highly efficient iodine capture: theoretical calculations and experimental verification.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.146660]
2. Jiahui Xu, Jia-qi Bai, Wenjie Si, Yunhai Zhang, Jiazhao Tan, Mengdie Cai, Qin Cheng, Song Sun.  (2023)  N,S-Co-doping Significantly Improves the Co–Nx Content of the Co-NSPC Catalyst and Enhances the Catalytic Performance for Selective Hydrogenation of Halogenated Nitrobenzenes.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.2c04127]
3. Xiaoyun Zhang, Yinhang Zhang, Yuxin Su, Xiaoyang Wang, Renqing Lv.  (2022)  Synthesis and Corrosion Inhibition Performance of Mannich Bases on Mild Steel in Lactic Acid Media.  ACS Omega,      [PMID:36120014] [10.1021/acsomega.2c03545]
4. Guo Lin, Shixing Wang, Libo Zhang, Tu Hu, Jinhui Peng, Song Cheng, Likang Fu, C. Srinivasakannan.  (2018)  Selective recovery of Au(III) from aqueous solutions using 2-aminothiazole functionalized corn bract as low-cost bioadsorbent.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2018.06.168]
5. Shihui Qiu, Gang Liu, Wei Li, Haichao Zhao, Liping Wang.  (2018)  Noncovalent exfoliation of graphene and its multifunctional composite coating with enhanced anticorrosion and tribological performance.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2018.03.007]
6. Chao Xiong, Shixing Wang, Libo Zhang, Ying Li, Yang Zhou, Jinhui Peng.  (2018)  Preparation of 2-Aminothiazole-Functionalized Poly(glycidyl methacrylate) Microspheres and Their Excellent Gold Ion Adsorption Properties.  Polymers,  10  (2): (159).  [PMID:30966195] [10.3390/polym10020159]
7. Gui-lin Zhuang, Jia-qi Bai, Xin-yong Tao, Jian-min Luo, Xiang Zhou, Wen-xian Chen, Xing Zhong, Xiao-nian Li, Jian-guo Wang.  (2017)  Trace phosphorus−doping significantly improving S-content of binary−doped mesoporous carbon network with enhancing electrochemical performance.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2017.07.054]
8. Binghai Wang, Juanqiang Wang, Qian Shao, Xingjun Xi, Qiao Chu, Genlai Dong, Yun Wei.  (2016)  Facile synthesis of thiazole-functionalized magnetic microspheres for highly specific separation of heme proteins.  NEW JOURNAL OF CHEMISTRY,  41  (2): (747-754).  [PMID:] [10.1039/C6NJ02755E]
9. Gui-lin Zhuang, Jia-qi Bai, Xin-yong Tao, Jian-min Luo, Xin-de Wang, Yi-fen Gao, Xing Zhong, Xiao-nian Li, Jian-guo Wang.  (2015)  Synergistic effect of S,N-co-doped mesoporous carbon materials with high performance for oxygen-reduction reaction and Li-ion batteries.  Journal of Materials Chemistry A,  (40): (20244-20253).  [PMID:] [10.1039/C5TA05252A]
10. Jiahui Xu, Xianlang Chen, Jia-qi Bai, Zhengan Miao, Yuan Tan, Nannan Zhan, Huangfei Liu, Mei Ma, Mengdie Cai, Qin Cheng, Song Sun.  (2024)  Efficient Co/NSPC catalyst for selective hydrogenation of halonitrobenzenes and mechanistic insight.  Catalysis Science & Technology,  14  (5): (1167-1180).  [PMID:] [10.1039/D3CY01767B]
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