Welcome to LookChem.com Sign In|Join Free
  • or
Carbamic acid, (4-chloro-2-nitrophenyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63379-20-4

Post Buying Request

63379-20-4 Suppliers

Recommended suppliers

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

63379-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63379-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,7 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63379-20:
(7*6)+(6*3)+(5*3)+(4*7)+(3*9)+(2*2)+(1*0)=134
134 % 10 = 4
So 63379-20-4 is a valid CAS Registry Number.

63379-20-4Downstream Products

63379-20-4Relevant academic research and scientific papers

Synthetic method of copper-catalyzed protective o-nitroaniline compounds

-

Paragraph 0028, (2018/04/28)

The invention discloses a synthetic method of copper-catalyzed protective o-nitroaniline compounds. The method comprises steps as follows: (1), protective phenylamine compounds serving as raw materials, oxidizing gas serving as an oxidant, any one of copp

A Comparison of the Reactions of Some Ethyl N-Arylcarbamates with Those of the Corresponding Acetanilides. I. Nitration

Rosevear, Judi,Wilshire, John F. K.

, p. 723 - 733 (2007/10/02)

The reactions of some ethyl N-arylcarbamates and of the corresponding acetanilides towards 1 equiv. of sodium nitrate in concentrated sulfuric acid at 0-5 deg have been compared with one another and have been found to exhibit significant differences.Except in the case of the unsubstituted analogues, nitration of the carbamates was found to occur significantly more quickly than that of the acetanilides as shown by (i) a representative competitive nitration, and (ii) the fact the carbamates containing a nitro group are nitrated smoothly whereas the corresponding nitroacetanilides are slow to react.On the basis of competitive reactions, it is suggested that this difference in reactivity is due to steric factors.

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 63379-20-4