Welcome to LookChem.com Sign In|Join Free
  • or
N-methyl-4-(prop-1-en-2-yl)aniline, also known as 4-(1-methylallyl)-N-methylaniline or 4-allyl-N-methylaniline, is an organic compound with the chemical formula C10H13N. It is a colorless to pale yellow liquid with a strong, pungent odor. N-methyl-4-(prop-1-en-2-yl)aniline is a derivative of aniline, featuring a methyl group attached to the nitrogen atom and a 1-methylallyl group (a three-carbon chain with a double bond and a methyl group) attached to the para position of the benzene ring. N-methyl-4-(prop-1-en-2-yl)aniline is used as an intermediate in the synthesis of various chemicals, including dyes, pharmaceuticals, and agrochemicals. It is also known for its potential applications in the production of polymers and as a chemical intermediate in the manufacturing of certain types of rubber. Due to its reactivity and the presence of a reactive double bond, it is important to handle N-methyl-4-(prop-1-en-2-yl)aniline with care, as it can undergo further chemical reactions.

1629-30-7

Post Buying Request

1629-30-7 Suppliers

Recommended suppliers

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

1629-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1629-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1629-30:
(6*1)+(5*6)+(4*2)+(3*9)+(2*3)+(1*0)=77
77 % 10 = 7
So 1629-30-7 is a valid CAS Registry Number.

1629-30-7Downstream Products

1629-30-7Relevant academic research and scientific papers

Palladium-catalyzed amination of aryl chlorides and bromides with ammonium salts

Green, Rebecca A.,Hartwig, John F.

, p. 4388 - 4391 (2014)

We report the palladium-catalyzed coupling of aryl halides with ammonia and gaseous amines as their ammonium salts. The coupling of aryl chlorides and ortho-substituted aryl bromides with ammonium sulfate forms anilines with higher selectivity for the primary arylamine over the diarylamine than couplings with ammonia in dioxane. The resting state for the reactions of aryl chlorides is different from the resting state for the reactions of aryl bromides, and this change in resting states is proposed to account for a difference in selectivities for reactions of the two haloarenes.

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 1629-30-7