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1-Methyl-4-(tributylstannyl)-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 179055-21-1 Structure
  • Basic information

    1. Product Name: 1-Methyl-4-(tributylstannyl)-1H-pyrazole
    2. Synonyms: 1-Methyl-4-(tributylstannyl)-1H-pyrazole;(1-Methyl-1H-pyrazol-4-yl)tributylstannane;1-Methyl-4-(tributylstannyl)-1H-pyrazole 97%
    3. CAS NO:179055-21-1
    4. Molecular Formula: C16H32N2Sn
    5. Molecular Weight: 371.14868
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 179055-21-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 126-128°C
    3. Flash Point: 149℃
    4. Appearance: /
    5. Density: 1.135 g/mL at 25 °C
    6. Refractive Index: n20/D1.563
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.25±0.10(Predicted)
    10. CAS DataBase Reference: 1-Methyl-4-(tributylstannyl)-1H-pyrazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-Methyl-4-(tributylstannyl)-1H-pyrazole(179055-21-1)
    12. EPA Substance Registry System: 1-Methyl-4-(tributylstannyl)-1H-pyrazole(179055-21-1)
  • Safety Data

    1. Hazard Codes: T,N
    2. Statements: 21-25-36/38-48/23/25-50/53
    3. Safety Statements: 35-36/37/39-45-60-61
    4. RIDADR: UN 2788 6.1/PG 3
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 179055-21-1(Hazardous Substances Data)

179055-21-1 Usage

Pyrazole derivative

A compound based on the pyrazole structure This indicates that the compound is derived from the pyrazole structure, which is a five-membered heterocyclic ring containing two nitrogen atoms.

Butylstannyl group at the 4-position

A functional group attached to the fourth position of the pyrazole ring This describes the specific location of the butylstannyl group on the pyrazole ring.

Methyl group at the 1-position

A functional group attached to the first position of the pyrazole ring This indicates the presence of a methyl group (a carbon atom with three hydrogen atoms) at the first position of the pyrazole ring.

Organic synthesis

Used in the synthesis of various organic compounds This highlights the compound's role in creating other organic molecules through chemical reactions.

Building block

A starting material for the preparation of other organic compounds This emphasizes the compound's importance as a fundamental component in the synthesis of other molecules.

Biological activities

Exhibits potential antitumor and antifungal properties This refers to the compound's ability to potentially inhibit the growth of tumors and fungi, making it a candidate for further research in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 179055-21-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,0,5 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 179055-21:
(8*1)+(7*7)+(6*9)+(5*0)+(4*5)+(3*5)+(2*2)+(1*1)=151
151 % 10 = 1
So 179055-21-1 is a valid CAS Registry Number.

179055-21-1 Well-known Company Product Price

  • Brand
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  • Aldrich

  • (707813)  1-Methyl-4-(tributylstannyl)-1H-pyrazole  97%

  • 179055-21-1

  • 707813-1G

  • 1,021.41CNY

  • Detail

179055-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tributyl-(1-methylpyrazol-4-yl)stannane

1.2 Other means of identification

Product number -
Other names 1-METHYL-4-(TRIBUTYLSTANNYL)-1H-PYRAZOLE

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:179055-21-1 SDS

179055-21-1Relevant articles and documents

METHODS OF TREATING CREATINE TRANSPORTER DEFICIENCY

-

Paragraph 0427-0428, (2021/10/02)

Disclosed are methods of treating creatine transporter deficiency, comprising administering to a mammal in need thereof a therapeutically effective amount of a compound that increases transport of a substrate by a mutant or wild-type creatine transporter. Also disclosed are methods of increasing transport of guanidinoacetic acid or a salt thereof across the blood-brain barrier of a mammal, and methods of decreasing accumulation or the concentration of guanidinoacetic acid or a salt thereof in a mammalian cell.

SMALL MOLECULES TARGETING MUTANT MAMMALIAN PROTEINS

-

Paragraph 0566-0567, (2021/12/03)

Disclosed are compounds, compositions, and methods useful for treating or preventing a disease or disorder associated with a mutation in a protein.

METHOD FOR PRODUCING 14 GROUP METAL LITHIUM COMPOUND

-

Paragraph 0085; 0087- 0088, (2016/10/31)

PROBLEM TO BE SOLVED: To provide a method for quantitatively producing a group 14 metal lithium compound under a mild condition. SOLUTION: The method for producing a group 14 metal lithium compound represented by formula (4): R4-nMLin comprises reacting a compound represented by formula (1): R4-nMXn and lithium in the presence of a polycyclic aromatic compound represented by formula (2) or formula (3). [In formula (1) and formula (2), R is a hydrocarbon group; M is a metal atom selected from Si, Ge and Sn; X is a halogen atom or R3M- (R and M are the same as mentioned above); and n is 1 or 2] and [R1 is H or a hydrocarbon group; and m is an integer of 0 to 5.] SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Stannyl-Lithium: A Facile and Efficient Synthesis Facilitating Further Applications

Wang, Dong-Yu,Wang, Chao,Uchiyama, Masanobu

supporting information, p. 10488 - 10491 (2015/09/28)

We have developed a highly efficient, practical, polycyclic aromatic hydrocarbon (PAH)-catalyzed synthesis of stannyl lithium (Sn-Li), in which the tin resource (stannyl chloride or distannyl) is rapidly and quantitatively transformed into Sn-Li reagent at room temperature without formation of any (toxic) byproducts. The resulting Sn-Li reagent can be stored at ambient temperature for months and shows high reactivity toward various substrates, with quantitative atom efficiency.

Vasopressin agonist formulation and process

-

Page/Page column 69, (2010/02/09)

This invention provides novel formulations for vasopressin agonist compounds, or a pharmaceutically acceptable salt thereof, having the general structure: and processes for making them, the formulations comprising from about 1% to about 20% of active ingredient, from about 1% to about 18% of a surfactant component, from about 50% to about 80% of a component of one or more polyethylene glycols, from about 1% to about 20% of a component of one or more sucrose fatty acid esters and/or polyvinylpyrrolidone and, optionally, one or more preservatives or antioxidants.

Tricyclic vasopressin agonists

-

, (2008/06/13)

This invention relates to new compounds selected from those of the general formula (I), or a pharmaceutically acceptable salt, ester or prodrug form thereof: wherein D, E and G are N or CH, which serve as vasopressin agonists and are useful in treating disorders such as diabetes insipidus, nocturnal enuresis, nocturia, urinary incontinence, bleeding and coagulation disorders, and the inability to temporarily delay urination and pharmaceutical compositions and methods for same.

Gamma-hydroxy-2-(fluoroalkylaminocarbonyl)-1-piperazinepentanamides and uses thereof

-

Page/Page column 181, (2010/01/31)

γ-Hydroxy-2-(fluoroalkylaminocarbonyl)-1-piperazinepentanamide compounds are inhibitors of HIV protease and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described. These compounds are effective against HIV viral mutants which are resistant to HIV protease inhibitors currently used for treating AIDS and HIV infection.

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