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Acetaldehyde, 2-benzothiazolylhydrazone (6CI,7CI,8CI,9CI) is a chemical compound with the molecular formula C9H10N4S. It is a derivative of acetaldehyde, where the aldehyde group has been converted into a hydrazone by reacting with 2-benzothiazolylhydrazine. Acetaldehyde, 2-benzothiazolylhydrazone (6CI,7CI,8CI,9CI) is often used as a reagent in analytical chemistry for the detection and determination of aldehydes and ketones. The 2-benzothiazolylhydrazone derivative provides a colored product upon reaction, which can be analyzed spectrophotometrically, making it a valuable tool for quantitative analysis in various fields, including pharmaceutical and environmental science.

3837-57-8

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3837-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3837-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3837-57:
(6*3)+(5*8)+(4*3)+(3*7)+(2*5)+(1*7)=108
108 % 10 = 8
So 3837-57-8 is a valid CAS Registry Number.

3837-57-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name acetaldehyde (2-benzothiazolyl)hydrazone

1.2 Other means of identification

Product number -
Other names N-Benzothiazol-2-yl-N'-eth-(E)-ylidene-hydrazine

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:3837-57-8 SDS

3837-57-8Relevant academic research and scientific papers

Pharmaceutical preparation

-

, (2008/06/13)

Pharmaceutical preparations having an antiphlogistic action are described. The preparations contain, as active ingredient, a benzazole derivative corresponding to the general tautomeric formulae I STR1 wherein X represents a sulphur or oxygen atom and R1 represents a hydrogen atom and R2 a hydroxymethyl, formyl, lower carbalkoxy or lower acyl group or R1 and R2 together represent the group STR2 wherein R3 and R4 denote, independently of one another, a hydrogen atom or a C1 -C6 -alkyl group, or they contain a physiologically acceptable salt thereof. These pharmaceutical preparations are suitable in particular for the treatment of inflammatory conditions and for inhibiting the lipoxygenase and/or cyclooxygenase route of arachidonic acid metabolism.

SYNTHESIS AND TRANSFORMATIONS OF S- AND N-SUBSTITUTED 2-MERCAPTOBENZOTHIAZOLES

Rutavichyus, A. I.,Iokubaitite, S. P.

, p. 33 - 36 (2007/10/02)

2-Mercaptobenzothiazole reacts with alkyl halides and hydrazine hydrate in the thiol form, and with formaldehyde in the thione form.The alkylation of 2-mercaptobenzothiazolidin-3-yl-methanol has been performed with sulfoalkyl halides and with propan-1,3-s

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