Dazomet - analytical standard, ≥97% , CAS No.533-74-4

CAS: 533-74-4 Cat. No.: D114733 Formula: C₅H₁₀N₂S₂ Peso molecolare: 162.28 Beilstein Registry Number: 116039 Numero EC: 208-576-7

QUALITÀ & PUREZZA Analytical standard, ≥97%

Synonyms

DAZOMET|533-74-4|Basamid|3,5-Dimethyl-1,3,5-thiadiazinane-2-thione|Tiazon|DMTT|Thiazone|Mylone|Dimethylformocarbothialdine|Carbothialdin|Nefusan|Prezervit|Thiazon|Crag nemacide|Basamid-Puder|Mico-fume|Crag 974|Basamid G|Basamid P|Basamide|Mylon|Mylone 85|

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifiche

Sinonimi

DAZOMET | 533-74-4 | Basamid | 3,5-Dimethyl-1,3,5-thiadiazinane-2-thione | Tiazon | DMTT | Thiazone | Mylone | Dimethylformocarbothialdine | Carbothialdin | Nefusan | Prezervit | Thiazon | Crag nemacide | Basamid-Puder | Mico-fume | Crag 974 | Basamid G | Basamid P | Basamide | Mylon | Mylone 85 |

Specifiche e purezza

analytical standard, ≥97%

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Standard analitico

Purezza

≥97%

Nomi e identificatori

Pubchem Sid

528772243

Sorrisi canonici

CN1CN(C(=S)SC1)C

IUPAC Name

3,5-dimethyl-1,3,5-thiadiazinane-2-thione

InChIKey

QAYICIQNSGETAS-UHFFFAOYSA-N

INCHI

1S/C5H10N2S2/c1-6-3-7(2)5(8)9-4-6/h3-4H2,1-2H3

Isomeri SMILES

CN1CN(C(=S)SC1)C

WGK Germania

3

RTECS

XI2800000

Numero UN

3077

Gruppo di imballaggio

III

Peso molecolare

162.28

Beilstein

116039

Reaxy-Rn

116039

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=116039&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Thiadiazinanes

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Thiadiazinanes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Thiadiazinanes
• Alternative Parents: Cyclic dithiocarbamic acid esters Thiohemiaminal derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Thiadiazinane - Cyclic dithiocarbamic acid ester - Dithiocarbamic acid ester - Azacycle - Hemithioaminal - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Organonitrogen compound - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as thiadiazinanes. These are organic heterocyclic compounds containing a six-membered saturated heterocycle with two nitrogen, one sulfur, and three carbon atoms.
• External Descriptors: Dithiocarbamate fungicides

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

Obiettivi associati (umani)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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RXRA Tclin Retinoid X receptor alpha (3637 Activities)

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PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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NCI-H358 (882 Activities)

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HepG2 (196354 Activities)

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Lymphoblastoid cell (5959 Activities)

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

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GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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SNCA Tchem Alpha-synuclein (10960 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

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SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)

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GMNN Tbio Geminin (128009 Activities)

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Obiettivi associati (non umani)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

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NS1 Nonstructural protein 1 (33327 Activities)

Discover Target: NS1

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Punto di infiammabilità (°F): 156 °C
• Punto di infiammabilità (°C): 156°C
• Punto di fusione (°C): 106-107°C
• Peso molecolare: 162.300 g/mol
• XLogP3: 1.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 162.029 Da
• Monoisotopic Mass: 162.029 Da
• Topological Polar Surface Area: 63.900 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 126.000
• 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