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(1-PHENYL-1H-TETRAZOL-5-YL)THIO]ACETIC ACID, also known as TATAC, is a chemical compound with the molecular formula C9H8N4OS. It is a thio derivative of tetrazole and is commonly used as a precursor in the synthesis of pharmaceuticals and organic compounds. TATAC is known to have anti-inflammatory and antioxidant properties, making it potentially useful in the development of drugs for the treatment of various medical conditions. Additionally, it is also used as a reagent in organic synthesis and chemical research due to its unique structure and capabilities. Overall, TATAC is an important chemical compound with a wide range of potential applications in the pharmaceutical and research industries.
Used in Pharmaceutical Industry:
(1-PHENYL-1H-TETRAZOL-5-YL)THIO]ACETIC ACID is used as a precursor in the synthesis of pharmaceuticals for its anti-inflammatory and antioxidant properties, making it potentially useful in the development of drugs for the treatment of various medical conditions.
Used in Research Industry:
(1-PHENYL-1H-TETRAZOL-5-YL)THIO]ACETIC ACID is used as a reagent in organic synthesis and chemical research for its unique structure and capabilities.

46505-33-3

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46505-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46505-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,5,0 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 46505-33:
(7*4)+(6*6)+(5*5)+(4*0)+(3*5)+(2*3)+(1*3)=113
113 % 10 = 3
So 46505-33-3 is a valid CAS Registry Number.

46505-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1-Phenyl-1H-tetrazol-5-yl)thio]acetic acid

1.2 Other means of identification

Product number -
Other names 5-hydrazino-1-phenyl-1H-tetrazole

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:46505-33-3 SDS

46505-33-3Relevant academic research and scientific papers

Synthesis and surface activity of some imidazole, 1,2,4-triazole, and tetrazole derivatives

Abramzon,Pevzner,Kofman,Alam

, p. 1841 - 1848 (2007/10/03)

Imidazole, 1,2,4-triazole, and tetrazole derivatives containing large alkyl substituents are prepared, and their surface activity is studied.

Tetrazoles. XXXI. Phase-Transfer Reactions of 1-Substituted Tetrazole-5-thiones and Their Derivatives

Gol'tsberg,Koldobskii

, p. 1194 - 1201 (2007/10/03)

Alkylation of 1-substituted tetrazole-5-thiones under conditions of phase-transfer catalysis in the two-phase system liquid-liquid proceeds regioselectively at the sulfur atom, regardless of the alkylating agent and phase-transfer catalyst. Phase-transfer oxidation of the 5-alkylthiotetrazoles thus obtained by potassium permanganate is a convenient method for preparation of 5-alkylsulfonyltetrazoles which can be used to synthesize functionally substituted tetrazoles.

Tetrazoles. XXXII. Reactions of 1-R-Tetrazole-5-Thiones and Their Derivatives under Conditions of Phase Transfer Catalysis. Selection of Phase Transfer Catalyst

Gol'tsberg,Grabalek,Farsa,Krebs,Dolezhal,Koldobsky

, p. 1367 - 1369 (2007/10/03)

Among the six investigated catalysts of phase transfer the most effective at alkylation of 1-phenyltetrazole-5-thione and oxidation of 5-methylthio-phenyltetrazole turned out to be the benzyldimetyhyl(5-methoxycarbonylpentyl)ammonium bromide. The directio

ANTIMYCOBACTERIAL DERIVATIVES OF TETRAZOLE

Waisser, Karel,Vanzura, Jiri,Hrabalek, Alexandr,Vinsova, Jarmila,Gresak, Stefan,et al.

, p. 2389 - 2394 (2007/10/02)

A synthesis of (1-phenyltetrazol-5-ylthio)acetic acid derivatives has been developed.Functional variations concern the carboxylic group and/or the 4 position of phenyl group.Most of the compounds prepared have been tested with regard to their antimycobact

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