Welcome to LookChem.com Sign In|Join Free
  • or
3-Hydroxy-2-methyl-1-phenyl-2-propen-1-one, also known as 2-methyl-1-phenyl-3-hydroxy-2-propen-1-one, is an organic compound with the molecular formula C10H10O2. It is a derivative of chalcone, a class of organic compounds that are open-chain isomers of flavonoids. This specific compound features a hydroxyl group (-OH) at the 3-position, a methyl group (-CH3) at the 2-position, and a phenyl ring (C6H5) attached to the 1-position of the propenone backbone. It is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals, fragrances, and other organic compounds. Due to its reactive nature, it is typically handled with care in controlled laboratory settings.

3516-69-6

Post Buying Request

3516-69-6 Suppliers

Recommended suppliers

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

3516-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3516-69-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3516-69:
(6*3)+(5*5)+(4*1)+(3*6)+(2*6)+(1*9)=86
86 % 10 = 6
So 3516-69-6 is a valid CAS Registry Number.

3516-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2-methyl-1-phenyl-2-propen-1-one

1.2 Other means of identification

Product number -
Other names -

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:3516-69-6 SDS

3516-69-6Relevant academic research and scientific papers

Synthesis of substituted benzenes from α-methylene ketones

Khaidem, Ibomacha Singh,Singh, Sagolsem Lokhol,Singh, Laishram Ramananda,Khan, Mohd Ziaur Rahman

, p. 911 - 914 (2007/10/03)

A new general method for the synthesis of substituted benzenes from cyclic ketones having active methylene groups via the corresponding hydroxymethylene ketones and enamino-ketones has been developed. Formylation of these ketones with ethyl formate followed by enamination with pyrrolidine produces enamino-ketones which on reaction with threefold excess of malononitrile in boiling benzene in the presence of ammonium acetate in acetic acid gives the substituted benzenes in good yield. The reaction has been extended to aliphatic and aromatic ketones having active methylene groups to give substituted benzenes and biphenyls, respectively.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3516-69-6