Welcome to LookChem.com Sign In|Join Free

CAS

  • or

500701-14-4

Post Buying Request

500701-14-4 Suppliers

Recommended suppliersmore

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

500701-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500701-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,0 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 500701-14:
(8*5)+(7*0)+(6*0)+(5*7)+(4*0)+(3*1)+(2*1)+(1*4)=84
84 % 10 = 4
So 500701-14-4 is a valid CAS Registry Number.

500701-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecyl-phenethyl-amine

1.2 Other means of identification

Product number -
Other names Dodecyl-phenaethyl-amin

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:500701-14-4 SDS

500701-14-4Downstream Products

500701-14-4Relevant articles and documents

Method for synthesizing N-alkyl-N-aryl (methyl) acrylamide double-tail hydrophobic monomer

-

Paragraph 0029; 0030, (2019/10/01)

The invention discloses a method for synthesizing an N-alkyl-N-aryl (methyl) acrylamide double-tail hydrophobic monomer. The method comprises the following steps: (1) putting alkylamine into a methanol solution with aromatic aldehyde, increasing the temperature till backflow, and performing a reaction over night; reducing the temperature of the mixed liquid to 5 DEG C or lower, adding a small amount of sodium borohydride for multiple times, removing an ice water bath, continuously performing a reaction for 30-120 minutes, and performing a backflow reaction for 3-6 hours; adding a certain amount of water to quench the reaction, drying an organic phase, and performing rotational evaporation so as to remove a solvent so as to obtain N-aryl-N-alkylamine; and (2) dissolving the N-aryl-N-alkylamine by using dichloromethane, adding a NaOH solution, slowly dropping a dichloromethane solution of (methyl) acryloyl chloride under a stirring condition of the ice water bath, performing heating to the room temperature, continuously performing a reaction for 2-12 hours, washing an organic layer till neutral by using distilled water, and further performing drying and rotational evaporation, so asto obtain N-alkyl-N-aryl (methyl) acrylamide. The method is gentle in reaction condition, short in reaction time, high in yield and applicable to large-scale industrial application.

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 500701-14-4