Welcome to LookChem.com Sign In|Join Free

CAS

  • or

120958-26-1

Post Buying Request

120958-26-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

120958-26-1 Usage

General Description

2-Propenal, 3-(2-Methoxyphenyl)-2-Methyl- is a chemical compound with the molecular formula C11H12O2. It is also known as o-Anisaldehyde, and it is a clear, pale yellow liquid with a strong, sweet, floral odor. This chemical is commonly used as a flavoring agent in the food and beverage industry, and it is also used in the production of perfumes and fragrances. Additionally, 2-Propenal, 3-(2-Methoxyphenyl)-2-Methyl- has been studied for its potential applications in pharmaceuticals and as a building block for organic synthesis. However, it is important to handle this chemical compound with caution, as it may cause irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 120958-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,5 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120958-26:
(8*1)+(7*2)+(6*0)+(5*9)+(4*5)+(3*8)+(2*2)+(1*6)=121
121 % 10 = 1
So 120958-26-1 is a valid CAS Registry Number.

120958-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(2-methoxyphenyl)-2-methylacrylaldehyde

1.2 Other means of identification

Product number -
Other names 3-(2-METHOXYPHENYL)-2-METHYL-2-PROPENAL

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:120958-26-1 SDS

120958-26-1Relevant articles and documents

Diastereoselective addition of methylmetal reagents to 2-methylaldehydes

Larsson, Michael,H?gberg, Hans-Erik

, p. 7541 - 7548 (2001)

The preparation of compounds incorporating the 3-hydroxy-2-methyl-1-butyl moiety of high diastereomeric purity is described. These compounds can serve as potential building blocks for the preparation of several kinds of natural products. The diastereoselective addition of a number of methylmetal derivatives to three 3-substituted 2-methylaldehydes in various solvents was studied. An excellent diastereomeric ratio (95:5 anti-Cram/Cram) was obtained with 2-methyl-3-(phenylsulfanyl)propanal (5) and Me2Zn in the presence of TiCl4.

Poly(phosphoric acid) (PPA)-Promoted 5- exo -Cyclization of Iminium Ions Generated in Situ: A Facile Access to Functionalized Indene Derivatives

Zhu, Yi-Fan,Geng, Xin-Le,Guan, Yong-Hong,Teng, Wei,Fan, Xiaohui

supporting information, p. 1821 - 1827 (2017/09/30)

A metal-free Bronsted acid promoted two-component reaction between cinnamaldehydes and sulfonamides is described. This cascade process provides a simple and atom-economical alternative synthesis of a range of functionalized indenes from easily available starting materials. The resulting N -indenylsulfonamides were readily converted into the corresponding indenylenamines or indanones.

Secondary amine catalyzed retro-aldol reactions of enals and enones: One-pot conversion of enals to α-substituted derivatives

Enders, Dieter,Nguyen, Thanh V.

experimental part, p. 2091 - 2095 (2012/07/14)

A practical synthetic procedure to hydrolytically cleave the C,C-double bond of α,β-unsaturated aldehydes and ketones has been developed. Secondary amines are employed as organocatalysts for the retro-aldol process under simple and mild reaction conditions. Beside the generation of the parent aromatic aldehydes, the synthetic procedure has been successfully used in a one-pot reaction sequence to convert simple cinnamaldehydes into their α-aryl/alkyl substituted derivatives.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 120958-26-1