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(1-METHYL-1 H-TETRAZOL-5-YLSULFANYL)-ACETIC ACID is a chemical compound with the molecular formula C5H7N5O2S. It is a white to off-white crystalline powder that is commonly used as a pharmaceutical intermediate in the synthesis of various medications. (1-METHYL-1 H-TETRAZOL-5-YLSULFANYL)-ACETIC ACID has been studied for its potential therapeutic applications, including its ability to act as a selective inhibitor of certain enzymes. Additionally, it has been investigated for its possible use in the treatment of cardiovascular and metabolic disorders. (1-METHYL-1 H-TETRAZOL-5-YLSULFANYL)-ACETIC ACID's structural and pharmacological properties make it a subject of interest for further research and potential medical applications.
Used in Pharmaceutical Industry:
(1-METHYL-1 H-TETRAZOL-5-YLSULFANYL)-ACETIC ACID is used as a pharmaceutical intermediate for the synthesis of various medications due to its unique structural and pharmacological properties.
Used in Enzyme Inhibition Applications:
(1-METHYL-1 H-TETRAZOL-5-YLSULFANYL)-ACETIC ACID is used as a selective inhibitor of certain enzymes, making it a potential candidate for the development of new therapeutic agents.
Used in Cardiovascular and Metabolic Disorder Treatment:
(1-METHYL-1 H-TETRAZOL-5-YLSULFANYL)-ACETIC ACID is being investigated for its potential use in the treatment of cardiovascular and metabolic disorders, offering a promising avenue for further research and medical applications.

55862-52-7

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55862-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55862-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,6 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55862-52:
(7*5)+(6*5)+(5*8)+(4*6)+(3*2)+(2*5)+(1*2)=147
147 % 10 = 7
So 55862-52-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4O2S/c1-8-4(5-6-7-8)11-2-3(9)10/h2H2,1H3,(H,9,10)

55862-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-methyltetrazol-5-yl)sulfanylacetic acid

1.2 Other means of identification

Product number -
Other names F1999-0010

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:55862-52-7 SDS

55862-52-7Relevant academic research and scientific papers

Synthesis and insecticidal activity of tetrazole-linked triazole derivatives

Maddila, Suresh,Pagadala, Ramakanth,Jonnalagadda, Sreekanth B.

, p. 487 - 491 (2015)

A new series of 4-(4-substitutedbenzylideneamino)-5-((1-methyl-1H-tetrazol-5-ylthio)methyl)-4H-1,2,4-triazole-3-thiol derivatives (5a, 5b, 5c, 5d, 5e, 5f, 5g, 5h, 5i, 5j, 5k) are prepared using 4-amino-5-((1-methyl-1H-tetrazol-5-ylthio)methyl-4H-1,2,4-triazole-3-thiol (4), as an intermediate compound. The structures of all the newly synthesized products are established supported by their spectral 1H NMR, 13C NMR, FTIR, electrospray ionization mass spectrometry (mass), and analytical data. All the compounds are screened for their insecticidal activity against Plodia interpunctella, and six compounds exhibited significant activity.

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.

SYNTHESIS OF 2-(HETEROCYCLYLTHIOMETHYL)PENEMS

Alpegiani, Marco,Bedeschi, Angelo,Franceschi, Giovanni,Giudici, Franco,Nannini, Giuliano,Perrone, Ettore

, p. 319 - 324 (2007/10/02)

The synthesis of representatives of an important class of penem antibiotics is described, exploiting a new procedure for preparing phosphoranes from base-sensitive chlorides and a purpose-tailored carboxyl protective group.Double bond migration out of the ring to give 2-(heterocyclylthiomethylene)penams was observed even in pH 7.4 phosphate buffer.

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