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Benzothiazole, 2-methyl-, hydrobromide (8CI,9CI) is a chemical compound with the molecular formula C8H8BrNS. It is a derivative of benzothiazole, a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. The 2-methyl group in Benzothiazole, 2-methyl-, hydrobromide (8CI,9CI) is attached to the benzene ring, and the hydrobromide ion (HBr) is present as a counterion. Benzothiazole, 2-methyl-, hydrobromide (8CI,9CI) is often used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is typically obtained through the reaction of 2-methylbenzothiazole with hydrobromic acid (HBr). Benzothiazole, 2-methyl-, hydrobromide is a colorless to pale yellow crystalline solid, soluble in water and various organic solvents. It is important to handle Benzothiazole, 2-methyl-, hydrobromide (8CI,9CI) with care, as it may have potential health hazards and should be stored away from heat and open flames.

874-45-3

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874-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874-45-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 874-45:
(5*8)+(4*7)+(3*4)+(2*4)+(1*5)=93
93 % 10 = 3
So 874-45-3 is a valid CAS Registry Number.

874-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylbenzothiazolium bromide

1.2 Other means of identification

Product number -
Other names 2-methyl-benzothiazole hydrobromide

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:874-45-3 SDS

874-45-3Downstream Products

874-45-3Relevant academic research and scientific papers

Crown ether styryl dyes: 21. Synthesis, spectral properties, and complex formation of trans-isomers of the chromogenic dithia-15(18)-crown-5(6) ethers

Gromov,Fedorova,Vedernikov,Fedorov,Alfimov

, p. 967 - 974 (1997)

Novel styryl dyes containing dithia-15(18)-crown-6(5)-ether moieties were synthesized. Their selective complex formation with Hg2+ and Ag+ ions was studied by 1H NMR and electronic spectroscopy; the stability constants of the Ag+ complexes and the relative stability constants (in relation to benzodithia-18-crown-6) of the Hg2+ complexes were determined. The chemical shifts of the β,β′-protons in the CH2S group change upon the complex formation in parallel with the logK1 values of the complexes.

Nucleic acid probe, method for designing nucleic acid probe, and method for detecting target sequence

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Page/Page column 56; 57, (2018/02/28)

The present invention provides a nucleic acid probe that can achieve high detection sensitivity and high specificity in mutation detection, mismatch detection, etc. by the PCR method, a method for designing such a nucleic acid probe, and a method for detecting a target sequence. The nucleic acid probe includes a nucleic acid molecule, and the nucleic acid molecule includes a plurality of fluorescent dye moieties that exhibit an excitonic effect. At least two of the fluorescent dye moieties that exhibit an excitonic effect are bound to the same base or two adjacent bases in the nucleic acid molecule with each fluorescent dye moiety being bound via a linker (a linking atom or a linking atomic group). The extension-side end of the nucleic acid molecule is chemically modified, thereby preventing an extension reaction of the nucleic acid molecule.

COMPOUND, NUCLEIC ACID, LABELING SUBSTANCE, AND DETECTION METHOD

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Paragraph 0195, (2015/09/28)

The present invention provides a compound represented by the following chemical formula (I); a tautomer or stereoisomer of the compound; or a salt of the compound, the tautomer, or the stereoisomer. In the chemical formula (I), R1 and R2

Synthesis and spectroscopic studies of novel photochromic benzodithiacrown ethers and their complexes

Alfimov, Michael V.,Fedorov, Yurii V.,Fedorova, Olga A.,Gromov, Sergey S.,Hester, Ronald E.,et al.

, p. 1441 - 1448 (2007/10/03)

New styryl dyes containing the benzodithia-18-crown-6 fragment have been synthesized and their photoisomerization reactions and complexes with Hg2+ and Ag+ cations have been investigated by steady-state electronic and resonance Raman

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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