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5,6-DIMETHYL-2,1,3-BENZOSELENADIAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2626-34-8

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2626-34-8 Usage

Safety Profile

Poison by intravenous route. When heated to decomposition it emits toxic fumes of NOx and Se.

Check Digit Verification of cas no

The CAS Registry Mumber 2626-34-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2626-34:
(6*2)+(5*6)+(4*2)+(3*6)+(2*3)+(1*4)=78
78 % 10 = 8
So 2626-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2Se/c1-5-3-7-8(4-6(5)2)10-11-9-7/h3-4H,1-2H3

2626-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dimethyl-2,1,3-benzoselenadiazole

1.2 Other means of identification

Product number -
Other names 5,6-dimethylbenzo-2,1,3-selenadiazole

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:2626-34-8 SDS

2626-34-8Downstream Products

2626-34-8Relevant academic research and scientific papers

Synthesis and study of charge-transfer complexes for 5,6- dimethyl-2,1,3-benzoselenadiazole

Hassan, Attard F.,Radhy, Hanan A.,Zayed

experimental part, p. 477 - 484 (2010/08/06)

THE SYNTHESIS.of new solid charge - transfer (CT) complexes using 5,6-dimethyl-2,l,3-benzosclnadiazoles as donors with 1,4naphthaquinone; 1,8-dihydroxy anthraquinone, 2-hydroxy-l,4naphthaquinone and 2,3-dichloro-4,5-dicyano p-benzoquinone (DDQ) as acceptor to obtain compounds I-IV, respectively are reported. These complexes are characterized by elemental analysis, IR, UV-Vis electronic, 1HNMR and ESR spectroscopic data. The conductivity for the solid complexes I-IV reveals that they are not conductors.

Structural and Nuclear Magnetic Resonance Studies of short Selenium - Nitrogen Bonds

Roesky, Herbert W.,Weber, Karl-Ludwig,Seseke, Ulrich,Pinkert, Waltraud,Noltemeyer, Mathias,et al.

, p. 565 - 572 (2007/10/02)

SeCl4 reacts with Ph3P=NSiMe3 (2) by elimination of SiMe3Cl to form Ph3P=NSeCl3 (3), which is converted to (Ph3P=N)2SeCl2 (4) by a further mole of (2).Compound (4) may also be prepared from (2) and SeOCl2 or Se2Cl2; (4) reacts with SbCl5 to from (Ph3P=N)

Formation and Rearrangement of Adducts from Benzyne and Substituted 2,1,3-Benzoselenadiazoles

Bryce, Martin R.,Reynolds, Colin D.,Hanson, Peter,Vernon, John M.

, p. 607 - 613 (2007/10/02)

A series of 5-(1,2-benzoselenazol-3-yl)pentadienonitrile derivatives (2) has been prepared by addition of benzyne to substituted 2,1,3-benzoselenadiazoles.Some of these adducts rearrange either thermally or photochemically to give 2-(2-pyridyl)phenyl selenocyanates (7), which are reduced to 2-phenylpyridine derivatives (6) or hydrolysed to give ultimately, diselenides (9).The crystal structure of one benzyne adduct (2b) is reported and the mechanism of its rearrangement discussed.

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