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13604-13-2

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13604-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13604-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,0 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13604-13:
(7*1)+(6*3)+(5*6)+(4*0)+(3*4)+(2*1)+(1*3)=72
72 % 10 = 2
So 13604-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NS2/c1-2-11-9-10-7-5-3-4-6-8(7)12-9/h2-6H,1H2

13604-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenylsulfanyl-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-Vinylmercapto-benzthiazol

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:13604-13-2 SDS

13604-13-2Relevant articles and documents

Controlled Synthesis of Thiazole-Based Polymers and Block Copolymers by RAFT Polymerization of Azolyl S-Vinyl Sulfides and Metal Complexation

Nakabayashi, Kazuhiro,Matsumura, Aiko,Abiko, Yohei,Mori, Hideharu

, p. 1616 - 1629 (2016)

We studied the RAFT polymerization of five S-vinyl sulfide derivatives containing azole units, including 2-benzothiazolyl vinyl sulfide (BTVS), 2-thiazolyl vinyl sulfide (2-TVS), 1,3,4-thiadiazolyl vinyl sulfide (1,3,4-TVS), 5-methyl-1,3,4-thiadiazolyl vi

Synthesis of alkylthio- and arylthioheteroarenes by regioselective grignard reaction of thiocyanatoheteroarenes

Nagasaki, Izuru,Matsumoto, Miyuki,Yamashita, Masanori,Miyashita, Akira

, p. 1015 - 1024 (2007/10/03)

Treatment of thiocyanatoheteroarenes (1) with Grignard reagents (2) afforded alkylthio- or arylthioheteroarenes (3-6) in good yields. Grignard reagents regioselectively attacked the sulfur atom of the thiocyanato group owing to the metal-chelating effect of this group in combination with the hetero ring-nitrogen. 2-Thiocyanatopyridine (1a), 2-thiocyanatopyrimidine (1b), 2-thiocyanatobenzothiazole (1c), and 4-thiocyanatoquinazoline (1d) were converted into a variety of sulfides. Sulfides consisting of two heteroarenes linked by a sulfur atom were readily obtained by this method.

GAS/SOLID-REACTIONS WITH SULFUR COMPOUNDS

Kaupp, Gerd,Luebben, Doris,Sauerland, Olaf

, p. 109 - 120 (2007/10/02)

The various types of gas/solid-reactions (addition, elimination, substitution, condensation, catalyzed cycloaddition) in different branches of sulfur chemistry (heterocycles, S-vinyl-compounds, thioethers, thiols, sulfur dioxide) are reviewed, new types a

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