Welcome to LookChem.com Sign In|Join Free

CAS

  • or

54951-55-2

Post Buying Request

54951-55-2 Suppliers

Recommended suppliersmore

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

54951-55-2 Usage

Appearance

Yellow crystalline solid

Odor

Characteristic

Physical state

Solid

Chemical classification

Nitro-substituted chalcone compound

Importance

Building block in the synthesis of various organic compounds

Industries

Pharmaceutical and chemical

Biological properties

Potential anticancer, antimicrobial, and anti-inflammatory properties

Applications

Drug development and medical research

Check Digit Verification of cas no

The CAS Registry Mumber 54951-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,5 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54951-55:
(7*5)+(6*4)+(5*9)+(4*5)+(3*1)+(2*5)+(1*5)=142
142 % 10 = 2
So 54951-55-2 is a valid CAS Registry Number.

54951-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-(4-nitrophenyl)pent-1-en-3-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:54951-55-2 SDS

54951-55-2Downstream Products

54951-55-2Relevant articles and documents

One single catalyst, Pd(OAc)2, for two sequential very different steps: Allylic alcohol oxidation-Heck reaction. Access to functionalised α,β-unsaturated ketones

Batt, Frederic,Gozzi, Christel,Fache, Fabienne

supporting information; experimental part, p. 5830 - 5832 (2009/04/13)

A single addition of the catalyst, Pd(OAc)2, was realised to mediate two transformations as different as allylic alcohol oxidation under O2 and C-C bond formation of the Heck type, to give substituted α,β-unsaturated ketones without intermediate purification. The Royal Society of Chemistry.

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 54951-55-2