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Benzamide, N-(1-piperidinylthioxomethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58415-38-6 Structure
  • Basic information

    1. Product Name: Benzamide, N-(1-piperidinylthioxomethyl)-
    2. Synonyms:
    3. CAS NO:58415-38-6
    4. Molecular Formula: C13H16N2OS
    5. Molecular Weight: 248.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58415-38-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzamide, N-(1-piperidinylthioxomethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, N-(1-piperidinylthioxomethyl)-(58415-38-6)
    11. EPA Substance Registry System: Benzamide, N-(1-piperidinylthioxomethyl)-(58415-38-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 58415-38-6(Hazardous Substances Data)

58415-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58415-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,1 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58415-38:
(7*5)+(6*8)+(5*4)+(4*1)+(3*5)+(2*3)+(1*8)=136
136 % 10 = 6
So 58415-38-6 is a valid CAS Registry Number.

58415-38-6Relevant articles and documents

Design, synthesis and identification of novel substituted 2-amino thiazole analogues as potential anti-inflammatory agents targeting 5-lipoxygenase

Sinha, Shweta,Doble, Mukesh,Manju

, p. 34 - 50 (2018/09/13)

Human 5-Lipoxygenase (5-LOX) is a key enzyme targeted for asthma and inflammation. Zileuton, the only drug against 5-LOX, was withdrawn from the market due to several problems. In the present study, the performance of rationally designed conjugates of thi

Expanding the donor-acceptor toolbox with a minimal 5-(thiophen-2-yl)-1,3-thiazole core: Transition metal-free synthesis and molecular design for HOMO-LUMO energy modulations

Radhakrishnan, Rakesh,Sreejalekshmi, Kumaran G.

supporting information, p. 3036 - 3039 (2016/05/09)

Synthesis of a minimal 5-(thiophen-2-yl)-1,3-thiazole core through a transition metal-free, versatile [4+1] route is reported. DFT calculations on a prototype library of D-A-D-A tetrads established the exquisite HOMO-LUMO energy modulation by varying peri

Crystal structures and antimicrobial and cytotoxic activities of zinc(II), nickel(II) and copper(II) complexes of N-(piperidylthiocarbonyl)benzamide

Xie, Juan,Cheng, Zhongqin,Yang, Wen,Liu, Huanhuan,Zhou, Weiqun,Li, Mengying,Xu, Yunlong

, p. 157 - 164 (2015/03/30)

A new zinc(II) complex of N-(piperidylthiocarbonyl)benzamide, [ZnL2], has been synthesized and characterized using elemental analysis, Fourier transform infrared and 1H NMR spectroscopies. X-ray diffraction indicates that [ZnL2

Crystal structures and antifungal activities of fluorine-containing thioureido complexes with nickel(II)

Li, Chun,Yang, Wen,Liu, Huanhuan,Li, Mengying,Zhou, Weiqun,Xie, Juan

, p. 15737 - 15749 (2014/01/17)

Ni(II) complexes with N-2-fluorobenzoylpiperidine-1-carbothioimidate (L2-), N-4-fluorobenzoylpiperidine-1-carbothioimidate (L3-), N-2- fluorobenzoylmorpholine- 1-carbothioimidate (L5-) and N-4- fluorobenzoylmorpholine-1-carbothioimidate (L6-) have been synthesized and characterized by elemental analysis, FTIR and 1H-NMR. The crystal structures of three ligands (HL2, HL3 and HL6) and the corresponding Ni(II) complexes ([Ni(L2)2], [Ni(L3)2] and [Ni(L6)2]) have been determined by X-ray diffraction. The antifungal activities of the Ni(II) complexes together and the corresponding ligands against the fungi Botrytis cinerea, Trichoderma spp., Myrothecium and Verticillium spp. have been investigated. The experimental results showed that the ligands and their complexes have antifungal abilities. When the fluorine was substituted on the para-benzoyl moiety, the antifungal activity of the ligands was obviously increased. Moreover, the ligands were stronger than their complexes in inhibiting fungal activities. The antifungal ability of HL6 is especially strong, and similar to that of the commercial fungicide fluconazole.

Efficient one-pot synthesis of alkyl 2-(dialkylamino)-4-phenylthiazole-5- carboxylates and single-crystal x-ray structure of methyl 2-(diisopropylamino)- 4-phenylthiazole-5-carboxylate

Souldozi, Ali,Ramazani, Ali,Dadrass, Ali Reza,Slepokura, Katarzyna,Lis, Tadeusz

scheme or table, p. 339 - 348 (2012/04/10)

The reaction between secondary amines, benzoyl isothiocyanate, and dialkyl acetylenedicarboxylates (=dialkyl but-2-ynedioates) in the presence of silica gel (SiO2) led to alkyl 2-(dialkylamino)-4-phenylthiazole-5- carboxylates in fairly high yi

Facile synthesis of 3-aryl/alkylamino 5-aryl/alkyl 1,2,4-oxadiazoles from acylthiourea

Chennakrishnareddy, Gundala,Debasis, Hazra,Jayan, Rapai,Manjunatha, Sulur G.

, p. 6170 - 6173 (2011/11/30)

Facile and selective synthesis of 3-aryl/alkylamino 5-aryl/alkyl 1,2,4-oxadiazoles starting from N-acylthioureas has been demonstrated. The regio-selectivity is achieved by simply selecting an appropriate base used for the generation of hydroxyl amine fro

A rapid, four-component synthesis of functionalized thiazoles

Sabbaghan, Maryam,Alidoust, Mostafa,Hossaini, Zinatossadat

, p. 824 - 828 (2012/04/23)

An efficient synthesis of 2-(dialkylamino)-4-phenyl)-1,3-thiazol-5-yl) (phenyl)methanone using acid chlorides, secondary amines, 2-bromoacethophenone and ammonium thiocyanate is described.

Silica-gel-catalyzed conversion of stabilized phosphorus ylides to benzo[e][1,3]thiazocin derivatives

Souldozi, Ali,Dadrass, Ali Reza

experimental part, p. 1921 - 1925 (2010/11/19)

The reaction between triphenylphosphine, dialkylacetylenedicarboxylates, and N-benzoyl thiourea derivatives leads to intermediates such as vinyltriphenylphosphonium salts, which undergo Michael addition to produce the highly functionalized phosphorus ylid

One-pot synthesis of functionalized thioureas by reaction of benzoyl isothiocyanates, secondary amines, and alkyl propiolates

Yavari, Issa,Sayyed-Alangi, S. Zahra,Sabbaghan, Maryam,Hajinasiri, Rahimeh,Iravani, Nasir

experimental part, p. 1025 - 1028 (2009/11/30)

An efficient one-pot synthesis of functionalized thioureas is described via three-component reaction of benzoyl isothiocyanates, secondary amines, and alkyl propiolates in the presence of triphenylphosphine (20∈mol%).

Versatile novel syntheses of imidazoles

Rolfs, Andreas,Liebscher, Juergen

, p. 3480 - 3487 (2007/10/03)

A novel ring transformation/desulfurization of substituted 2-methyl-1,2,4-thiadiazolium salts 2 provides a versatile entry to imidazoles 3 with a variety of substituents. Simple one-pot procedures combine the preparation of starting 1,2,4-thiadiazolium salts 2 from N-(thiocarbonyl)-N'-methylamidines 1 or 1,2,4-dithiazolium triiodides 6 with the ring transformation/desulfurization to the imidazoles 3. Alternatively, N-(thiocarbonyl)-N'-methylamidines 1 can be transformed to imidazoles 3 or to 1-substituted imidazoles 5 via S-methylation and elimination of methylthiol. In the same manner, a new entry to 4H-imidazoles 8 could be developed.

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