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Pyridine,2-[(2-propynyloxy)methyl]-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128813-27-4 Structure
  • Basic information

    1. Product Name: Pyridine,2-[(2-propynyloxy)methyl]-(9CI)
    2. Synonyms: Pyridine,2-[(2-propynyloxy)methyl]-(9CI)
    3. CAS NO:128813-27-4
    4. Molecular Formula: C9H9NO
    5. Molecular Weight: 147.17386
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 128813-27-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Pyridine,2-[(2-propynyloxy)methyl]-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyridine,2-[(2-propynyloxy)methyl]-(9CI)(128813-27-4)
    11. EPA Substance Registry System: Pyridine,2-[(2-propynyloxy)methyl]-(9CI)(128813-27-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 128813-27-4(Hazardous Substances Data)

128813-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128813-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,1 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 128813-27:
(8*1)+(7*2)+(6*8)+(5*8)+(4*1)+(3*3)+(2*2)+(1*7)=134
134 % 10 = 4
So 128813-27-4 is a valid CAS Registry Number.

128813-27-4SDS

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-(prop-2-ynoxymethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2-(2-Propynyloxymethyl)pyridine

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:128813-27-4 SDS

128813-27-4Downstream Products

128813-27-4Relevant articles and documents

Inhibitors against Fungal Cell Wall Remodeling Enzymes

Delso, Ignacio,Valero-Gonzalez, Jessika,Gomollón-Bel, Fernando,Castro-López, Jorge,Fang, Wenxia,Navratilova, Iva,van Aalten, Daan M. F.,Tejero, Tomás,Merino, Pedro,Hurtado-Guerrero, Ramon

, p. 128 - 132 (2018)

Fungal β-1,3-glucan glucanosyltransferases are glucan-remodeling enzymes that play important roles in cell wall integrity, and are essential for the viability of pathogenic fungi and yeasts. As such, they are considered possible drug targets, although inh

Enantioselective Palladium-Catalyzed Hydrophosphinylation of Allenes with Phosphine Oxides: Access to Chiral Allylic Phosphine Oxides

Wang, Jun,Yang, Zhiping

supporting information, p. 27288 - 27292 (2021/11/17)

A Pd-catalyzed hydrophosphinylation of alkyl and aryl-oxyallenes with phosphine oxides has been developed for the efficient and rapid construction of a family of chiral allylic phosphine oxides with a diverse range of functional groups. This methodology was further applied in the facile construction of chiral 2H-chromene and later stage functionalization of cholesterol.

2 - (1 ', 2', 3 '- Triazole - 4' - methyl pyridine oxyalkylene) - 1, 3, 4, 6 - O - acetyl - D - glucose and its preparation method and application

-

Paragraph 0024; 0033; 0034, (2018/04/01)

The invention discloses 2-(1',2',3'-triazolyl-4'-oxymethylenepyridyl)-1,3,4,6-O-acetyl-D-glucose with anti-rectal cancer activity. The 2-(1',2',3'-triazolyl-4'-oxymethylenepyridyl)-1,3,4,6-O-acetyl-D-glucose has a core structure of 1,3,4,6-O-acetyl-D-glucose subjected to 1,2,4-triazole derivative 2-site substitution. The above compound has good rectal cancer cell inhibition activity and can be used as a drug for resisting rectal cancer. A compound synthesis method comprises that 2-amino-D-glucose hydrochloride and an azidation reagent as raw materials undergo a reaction under alkaline conditions to produce a 2-azido-1,3,4,6-O-acetyl-D-glucose intermediate, 3-propargyl bromide and aromatic methanol undergo a reaction under the action of sodium hydride to produce aromatic propargyl ether, and the 2-azido-1,3,4,6-O-acetyl-D-glucose intermediate and the aromatic propargyl ether undergo a click reaction in a solvent in the presence of monovalent copper as a catalyst to produce 2-(1', 2', 3'-triazolyl-4'-oxymethylenepyridyl)-1,3,4,6-O-acetyl-D-glucose.

Dihydroisobenzofurans and isoindolines by intramolecular inverse Diels-Alder reactions of pyridines

Biedrzycki, Marek,De Bie, Dick A.,Van Der Plas, Henk C.

, p. 607 - 614 (2007/10/02)

Pyridines being substituted at position 2 or 3 with a silylated propynyloxymethyl side-chain undergo a thermolytic intramolecular Diels-Alder reaction with formation of dihydroisobenzofurans. The 3-substituted pyridines are found to be more reactive than

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