Welcome to LookChem.com Sign In|Join Free

CAS

  • or

104869-86-5

Post Buying Request

104869-86-5 Suppliers

Recommended suppliersmore

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

104869-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104869-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,6 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104869-86:
(8*1)+(7*0)+(6*4)+(5*8)+(4*6)+(3*9)+(2*8)+(1*6)=145
145 % 10 = 5
So 104869-86-5 is a valid CAS Registry Number.

104869-86-5SDS

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 2-(4-nitrophenyl)pentan-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:104869-86-5 SDS

104869-86-5Downstream Products

104869-86-5Relevant articles and documents

Visible-light-mediated α-arylation of enol acetates using aryl diazonium salts

Hering, Thea,Hari, Durga Prasad,Koenig, Burkhard

, p. 10347 - 10352 (2013/01/15)

Visible light mediates efficiently the α-arylation of enol acetates by aryl diazonium salts under mild conditions using [Ru(bpy)3]Cl 2 as a photoredox catalyst. The broad scope of the reaction toward various diazonium salts and enol acetates was explored. The application of this reaction in the concise synthesis of 2-substituted indoles was demonstrated

NUCLEOPHILIC SUBSTITUTION p-DINITROBENZENE WITH SOME CARBANIONS. FORMATION OF p-SUBSTITUTED NITROBENZENES

Iwasaki, Genji,Saeki, Seitaro,Hamana, Masatomo

, p. 31 - 34 (2007/10/02)

Treatment of p-dinitrobenzene with active methylene compounds of rather weak acidity in the presence of t-BuOK in liq NH3 at -70'C leads to nucleophilic substitution of a nitro group, giving p-substituted nitrobenzenes in generally good yields.

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 104869-86-5