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152407-52-8

4-nitrobenzaldehyde 1,3-benzothiazol-2-ylhydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 152407-52-8 Structure

  • Basic information

    1. Product Name: 4-nitrobenzaldehyde 1,3-benzothiazol-2-ylhydrazone
    2. Synonyms: 4-nitrobenzaldehyde 1,3-benzothiazol-2-ylhydrazone
    3. CAS NO:152407-52-8
    4. Molecular Formula: C14H10N4O2S
    5. Molecular Weight: 298.3198
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152407-52-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-nitrobenzaldehyde 1,3-benzothiazol-2-ylhydrazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-nitrobenzaldehyde 1,3-benzothiazol-2-ylhydrazone(152407-52-8)
    11. EPA Substance Registry System: 4-nitrobenzaldehyde 1,3-benzothiazol-2-ylhydrazone(152407-52-8)

  • 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: 152407-52-8(Hazardous Substances Data)

152407-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152407-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 152407-52:
(8*1)+(7*5)+(6*2)+(5*4)+(4*0)+(3*7)+(2*5)+(1*2)=108
108 % 10 = 8
So 152407-52-8 is a valid CAS Registry Number.

152407-52-8Relevant articles and documents

STRUCTURE OF 2-BENZOTHIAZOLYLHYDRAZONES OF AROMATIC AND ALIPHATIC ALDEHYDES

Shmelev, L. V.,Ol'khovikova, N. B.,Pervova, I. G.,Lipunova, G. N.,Orlova, E. E.,Lipunov, I. N.

, p. 472 - 479 (1993)

On the basis of data of 13C and 1H NMR and IR spectroscopy, it was shown that 2-benzothiazolylhydrazones of aliphatic aldehydes were in solution as a mixture of E and Z isomers, and hydrazones of aromatic aldehydes were in solution only as E isomers.All i

Arylhydrazones Derivatives Containing a Benzothiazole Moiety, Efficient Ligands in the Palladium-Catalyzed Mizoroki–Heck and Suzuki–Miyaura Cross-coupling Reactions under IR Irradiation

Ortega-Jiménez, Fernando,Penieres-Carrillo, José Guillermo,López-Cortés, José Guadalupe,Carmen Ortega-Alfaro,Lagunas-Rivera, Selene

, p. 1881 - 1888 (2017/09/12)

A simple arylhydrazone containing the benzothiazole moiety which may be used as an efficient ligand in the palladium-catalyzed Mizoroki–Heck and Suzuki–Miyaura cross-coupling reactions, under infrared irradiation as an alternative source of energy, is presented. The reactions proceeded with extremely high efficiency under mild conditions and produced very good yields.

Synthesis of new triazolo and pyrazolo benzothiazoles

Deshmukh,Patil,Jadhav,Shejwal

, p. 163 - 166 (2013/09/23)

Benzothiazole-2-thiol 1 on heating with excess of hydrazine hydrate yields 2-hydrazino-1,3-benzothiazole (2). Compound 2 on reaction with carbon disulfide in alkaline medium affords [1,2,4] triazolo [3,4-b] [1,3] benzothiazole-3-thiol (3). Condensation of 2 with various substituted aryl aldehydes yields corresponding hydrazine derivatives (4), which on cyclisation with acetic anhydride gave corresponding [1,2,4] triazolo [3,4-6] [1,3] benzothiazoles (5). Some other triazolo derivatives (6,7,8) of benzothiazole were obtained by the cyclization of 2 with benzoyl chloride, acetyl chloride and formic acid respectively. Again compound 2 on condensation with acetyl acetone and ethylacetoacetate gives pyrazolo derivatives (9,10) respectively. The synthesized compounds were characterized by elemental and spectral analysis.

Preparation and Spectroscopic Properties of 2-Benzothiazolyl Araldehyde Hydrazones

Hearn, Michael J.,Schulz, Jeannette,Sinha, Anvita,Collins, Pamela,Hallenbeck, Susan,Kustin, Michael

, p. 521 - 524 (2007/10/02)

Notwithstanding its tendency toward air oxidation in solution, 2-hydrazinobenzothiazole I reacted with aromatic aldehydes in ethanol to give the corresponding hydrazones III-XV in high yields and analytical purity.In related examples, acylation took place

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