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2-Benzothiazolamine, N-[[4-(dimethylamino)phenyl]methylene]-, also known as 2-(4-Dimethylaminobenzylidene)benzothiazolamine, is a chemical compound with the molecular formula C16H16N2S. It is a derivative of benzothiazole, featuring a dimethylamino group attached to a phenyl ring that is connected to the benzothiazole core through a methylene bridge. 2-Benzothiazolamine,N-[[4-(dimethylamino)phenyl]methylene]- is often used as an intermediate in the synthesis of various pharmaceuticals and dyes due to its unique chemical structure and reactivity. It is characterized by its yellow crystalline appearance and is sensitive to light, which can lead to degradation. The compound's properties make it a valuable building block in the creation of more complex molecules with specific applications in the chemical and pharmaceutical industries.

38248-49-6

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38248-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38248-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,4 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38248-49:
(7*3)+(6*8)+(5*2)+(4*4)+(3*8)+(2*4)+(1*9)=136
136 % 10 = 6
So 38248-49-6 is a valid CAS Registry Number.

38248-49-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(dimethylamino)phenylmethylidene]-1,3-benzothiazol-2-amine

1.2 Other means of identification

Product number -
Other names N-(4-(dimethylamino)benzylidene)benzothiazol-2-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38248-49-6 SDS

38248-49-6Relevant academic research and scientific papers

Ultrasound-assisted one-pot synthesis of bis-azetidinones in the presence of zeolite

Jetti, Venkateshwarlu,Chidurala, Praveen,Pagadala, Ramakanth,Meshram, Jyotsna S.,Ramakrishna, Chowdam

, p. E183-E188 (2014/11/08)

Sonochemical method is an innovative task for the sustainable chemical research industry. In this work, an attempt was made to synthesize bis-azetidin-2-ones (2a, 2b, 2c, 2d, 2e, 2f, 2g, 2h, 2i, 2j) by Staudinger reaction ([2 + 2] ketene-imine cycloadditi

Synthesis, spectroscopic and physicochemical investigations of environmentally benign heterocyclic Schiff base derivatives as antibacterial agents on the bases of in vitro and density functional theory

Asiri, Abdullah M.,Khan, Salman A.,Marwani, Hadi M.,Sharma, Kamlesh

, p. 82 - 89 (2013/05/21)

A series of Schiff bases were synthesized by the reaction of 4-dimethylamino-benzaldehyde and corresponding active amines under microwave irradiation. Results obtained from spectroscopic (FT-IR, 1H NMR, 13C NMR, GC-MS) and elemental

Synthesis and biological significance of 2-aminobenzothiazole derivatives

Srivastava,Shukla

experimental part, p. 306 - 309 (2009/05/31)

Several new 2-N-(substituted benzyledine)-imino-1,3-benzothiazole 1; 2-[2′-(substituted phenyl)-4′-oxo-1′,3′-thiazolidine]-1, 3-benzothiazole 2 and 2-[5′-(arylidene)-2′-substituted phenyl-4′-oxo-1′,3′-thiazolidine]-1,3-benzothiazole 3 have been synthesize

H NMR, IR and UV/VIS spectroscopic studies of some Schiff bases derived from 2-aminobenzothiazole and 2-amino-3-hydroxypyridine

Issa, Raafat M.,Khedr, Abdalla M.,Rizk, Helen

body text, p. 875 - 884 (2009/12/04)

By condensing 2-aminobenzothiazole with 2-hydroxy-1-naphthaldehyde, 2-hydroxybenzaldehyde, 4-methoxybenzaldehyde, 4-hydroxybenzal-dehyde, benzaldehyde and 4-dimethylaminobenzaldehyde, and five Schiff bases Ia-Ie are prepared. Also, two Schiff bases IIa an

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