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(E)-2-(2-nitroprop-1-en-1-yl) phenol is an organic compound characterized by its molecular formula C9H9NO3. (E)-2-(2-nitroprop-1-en-1-yl) phenol features a phenol group (C6H5OH) with a nitropropenyl group attached at the 2-position. The nitropropenyl group consists of a propene (C3H6) chain with a nitro group (NO2) at the 2-position. The "E" in the name indicates that the molecule has a trans configuration, meaning the nitro group and the phenol group are on opposite sides of the double bond. (E)-2-(2-nitroprop-1-en-1-yl) phenol is known for its potential applications in the synthesis of various chemical products and may exhibit reactivity due to the presence of the nitro group, which can participate in reduction and substitution reactions. It is important to handle such compounds with care due to the potential hazards associated with nitro-containing compounds.

86029-73-4

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86029-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86029-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86029-73:
(7*8)+(6*6)+(5*0)+(4*2)+(3*9)+(2*7)+(1*3)=144
144 % 10 = 4
So 86029-73-4 is a valid CAS Registry Number.

86029-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-hydroxyphenyl)-2-nitroprop-1-ene

1.2 Other means of identification

Product number -
Other names 2-(2-Nitro-propenyl)-phenol

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:86029-73-4 SDS

86029-73-4Relevant academic research and scientific papers

Phosphine-Catalyzed Chemoselective Reduction/Elimination/Wittig Sequence for Synthesis of Functionalized 3-Alkenyl Benzofurans

Liou, Yan-Cheng,Wang, Heng-Wei,Edukondalu, Athukuri,Lin, Wenwei

, p. 3064 - 3069 (2021)

An efficient protocol for the construction of functionalized 3-alkenyl benzofurans is demonstrated under metal-free conditions using catalytic amount of phosphine proceeding an intramolecular Wittig reaction. This one-pot reaction initiated by the phospha

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