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14366-33-7

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14366-33-7 Usage

General Description

The chemical compound {[(2-phenylhydrazino)carbonothioyl]sulfanyl}acetic acid is a complex organic molecule containing a phenylhydrazine group, a carbonothioyl functional group, and an acetic acid moiety. It is commonly used as a reagent in organic synthesis and pharmaceutical research. With its unique structure, this chemical may exhibit various biological activities and therapeutic potentials. Its chemical properties make it suitable for a wide range of applications, including in the development of new pharmaceuticals and the study of organic reactions. Overall, {[(2-phenylhydrazino)carbonothioyl]sulfanyl}acetic acid is a versatile compound with potential applications in various fields of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 14366-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,6 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14366-33:
(7*1)+(6*4)+(5*3)+(4*6)+(3*6)+(2*3)+(1*3)=97
97 % 10 = 7
So 14366-33-7 is a valid CAS Registry Number.

14366-33-7SDS

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-(anilinocarbamothioylsulfanyl)acetic acid

1.2 Other means of identification

Product number -
Other names -

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:14366-33-7 SDS

14366-33-7Relevant articles and documents

RING-CHAIN AND RING-LINEAR-RING TAUTOMERISM IN THIOCARBONOHYDRAZONES

Alekseev, V. V.,Zelenin, K. N.,Terent'ev, P. B.,Lashin, V. V.,Khorseeva, L. A.,Bulakhov, G. A.

, p. 491 - 501 (2007/10/02)

The structure of the thiocarbonohydrazones of monocarbonyl compounds was studied by 1H and 13C NMR spectroscopy in solutions and by mass spectrometry in the gas phase. In solutions, irrespective of the substitution in the aromatic ring and in the hydrazine fragment, the thiocarbonohydrazones of aromatic aldehydes exist in the linear form, whereas the 2- and 5-substituted thiocarbonohydrazones of ketones are susceptible to ring-chain tautomerism: Thiocarbonohydrazone - 4-amino-1,2,4-triazolidine-3-thione. Those not having substituents at the nitrogen atoms are susceptible to ring-linear-ring equilibria: Hexahydro-1,2,4,5-tetrazine-3-thione - thiocarbonohydrazone - 4-amino-1,2,4-triazolidine-3-thione. In the gas phase under conditions of high vacuum, according to the mass spectra, the coexistence of four tautomeric forms (linear, tetrazine, triazolidine, and 2-hydrazino-1,3,4-thiadiazolidine) is possible in individual cases.

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