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120277-39-6

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120277-39-6 Usage

General Description

2-Propen-1-ol, 3-(3-pyridinyl)-, (2E)-(9CI) is a chemical compound with the molecular formula C8H9NO. It is also known by the name 3-vinylpyridine and is classified as an unsaturated alcohol. This chemical is commonly used in the production of pharmaceuticals, as well as in the synthesis of various chemical compounds. It is also used as a reagent in organic synthesis and as a raw material in the production of surfactants and polymers. Additionally, 2-Propen-1-ol, 3-(3-pyridinyl)-, (2E)-(9CI) is used in the manufacturing of flavors and fragrances, making it a versatile chemical with a range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 120277-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,7 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120277-39:
(8*1)+(7*2)+(6*0)+(5*2)+(4*7)+(3*7)+(2*3)+(1*9)=96
96 % 10 = 6
So 120277-39-6 is a valid CAS Registry Number.

120277-39-6SDS

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 (2E)-3-(3-Pyridinyl)-2-propen-1-ol

1.2 Other means of identification

Product number -
Other names 3-Pyridin-2-ylacrolein

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:120277-39-6 SDS

120277-39-6Relevant articles and documents

Photoredox Activation of SF6for Fluorination

McTeague, T. Andrew,Jamison, Timothy F.

supporting information, p. 15072 - 15075 (2016/11/25)

We report the first practical use of SF6as a fluorinating reagent in organic synthesis. Photoredox catalysis enables the in situ conversion of SF6, an inert gas, into an active fluorinating species by using visible light. Under these conditions, deoxyfluorination of allylic alcohols is effected with high chemoselectivity and is tolerant of a wide range of functional groups. Application of the methodology in a continuous-flow setup achieves comparable yields to those obtained with a batch setup, while providing drastically increased material throughput of valuable allylic fluoride products.

Pd-catalyzed enantioselective allyl-allyl cross-coupling

Zhang, Ping,Brozek, Laura A.,Morken, James P.

supporting information; scheme or table, p. 10686 - 10688 (2010/11/04)

The Pd-catalyzed cross-coupling of allylic carbonates and allylB(pin) is described. The regioselectivity of this reaction is sensitive to the bite angle of the ligand, with small-bite-angle ligands favoring the branched substitution product. This mode of

3-Descladinosyl-6-O-carbamoyl and 6-O-carbonoyl macrolide antibacterial agents

-

Page/Page column 57-58, (2010/02/05)

3-Descladinosyl-6-O-carbamoyl and 6-O-carbonoyl macrolide antibacterial agents of the formula: wherein R1, W, R3, R4, R5, R6, X, X′, and Z are as described herein and in which the substituents have th

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