2-Methyl-2-thiazoline - ≥97% , CAS No.2346-00-1

CAS: 2346-00-1 Cat. No.: M103076 Peso molecular: 101.17 Beilstein Registry Number: 104274 Número EC: 219-071-6

GRADE & PURITY ≥97%

Synonyms

2-Methyl-2-thiazoline, 8CI | DTXSID1062336 | 2-Methyl-2-thiazoline, 98% | 2-Methyl-2-thiazoline, analytical standard | EN300-20730 | 2-Methyl-4,5-dihydro-1,3-thiazole | BRN 0104274 | C4H7NS | SCHEMBL208968 | 2-methyl-4,5-dihydrothiazole | 2-Methyl-4,5-dih

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

Meyers reagent for aldehyde synthesis.

Specifications

Sinónimos

2-Methyl-2-thiazoline, 8CI | DTXSID1062336 | 2-Methyl-2-thiazoline, 98% | 2-Methyl-2-thiazoline, analytical standard | EN300-20730 | 2-Methyl-4, 5-dihydro-1, 3-thiazole | BRN 0104274 | C4H7NS | SCHEMBL208968 | 2-methyl-4, 5-dihydrothiazole | 2-Methyl-4, 5-dih

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504752783
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752783
• Sonrisas canónicas: CC1=NCCS1
• IUPAC Name: 2-methyl-4,5-dihydro-1,3-thiazole
• InChIKey: JUIQOABNSLTJSW-UHFFFAOYSA-N
• INCHI: 1S/C4H7NS/c1-4-5-2-3-6-4/h2-3H2,1H3
• Isómeros SMILES: CC1=NCCS1
• WGK Alemania: 2
• RTECS: XJ4261470
• Número ONU: 1993
• Peso molecular: 101.17
• Beilstein: 104274
• Reaxy-Rn: 104274
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=104274&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Azolines
      • Subclass Thiazolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Azolines
• Subclass: Thiazolines
• Intermediate Tree Nodes: Not available
• Direct Parent: Thiazolines
• Alternative Parents: Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Meta-thiazoline - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as thiazolines. These are heterocyclic compounds containing a five-member unsaturated aliphatic ring with one nitrogen atom, one sulfur atom, three carbon atoms.
• External Descriptors: Not available

Data sources

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

Propiedades químicas y físicas

• Sensibilidad: heat sensitive; light sensitive;air sensitive
• Índice de refracción: 1.52
• Punto de inflamación (°F): 98.6 °F
• Punto de inflamación (°C): 37 °C
• Punto de ebullición (°C): 144.0-145.0°C
• Punto de fusión (°C): -101.0°C
• Peso molecular: 101.170 g/mol
• XLogP3: 0.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 101.03 Da
• Monoisotopic Mass: 101.03 Da
• Topological Polar Surface Area: 37.700 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 77.600
• 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

Referencias

1. Linhui Feng, Heping Cui, Pusen Chen, Khizar Hayat, Xiaoming Zhang, Chi-Tang Ho.  (2022)  Promoted Formation of Pyrazines and Sulfur-Containing Volatile Compounds through Interaction of Extra-Added Glutathione or Its Constituent Amino Acids and Secondary Products of Thermally Degraded N-(1-Deoxy-d-ribulos-1-yl)-Glutathione.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:35838405] [10.1021/acs.jafc.2c02949]

2. Bin Wu, Ling Meng, Yan Zhao, Junjie Li, Qiuyun Tian, Yayan Pang, Chunguang Ren, Zhifang Dong.  (2024)  Meningeal neutrophil immune signaling influences behavioral adaptation following threat.  NEURON,      [PMID:39561768] [10.1016/j.neuron.2024.10.018]