Welcome to LookChem.com Sign In|Join Free
  • or
4-methyl-1-(prop-2-en-1-yl)-1H-imidazole is an organic compound with the molecular formula C7H10N2. It is a derivative of imidazole, a heterocyclic aromatic organic compound containing two nitrogen atoms at positions 1 and 3. The structure of 4-methyl-1-(prop-2-en-1-yl)-1H-imidazole features a methyl group (-CH3) at the 4-position and a prop-2-en-1-yl group (CH2=CH-CH3) at the 1-position, which is attached to the imidazole ring. 4-methyl-1-(prop-2-en-1-yl)-1H-imidazole is known for its potential applications in various chemical and pharmaceutical industries, such as in the synthesis of agrochemicals and pharmaceuticals. It is also used as an intermediate in the production of certain drugs and as a building block in the synthesis of more complex molecules. Due to itsactivity re and unique structure, 4-methyl-1-(prop-2-en-1-yl)-1H-imidazole is a valuable chemical in the field of organic chemistry.

6307-15-9

Post Buying Request

6307-15-9 Suppliers

Recommended suppliers

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

6307-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6307-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6307-15:
(6*6)+(5*3)+(4*0)+(3*7)+(2*1)+(1*5)=79
79 % 10 = 9
So 6307-15-9 is a valid CAS Registry Number.

6307-15-9SDS

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 4-methyl-1-prop-2-enylimidazole

1.2 Other means of identification

Product number -
Other names 4-methyl-1-(prop-2-en-1-yl)-1h-imidazole

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:6307-15-9 SDS

6307-15-9Downstream Products

6307-15-9Relevant academic research and scientific papers

Palladium-Catalyzed Dehydrative Cross-Coupling of Allylic Alcohols and N-Heterocycles Promoted by a Bicyclic Bridgehead Phosphoramidite Ligand and an Acid Additive

Kang, Kyungjun,Kim, Jaewook,Lee, Ansoo,Kim, Woo Youn,Kim, Hyunwoo

supporting information, p. 616 - 619 (2016/02/18)

A mild and efficient dehydrative cross-coupling reaction between allylic alcohols and N-heterocycles using palladium catalysis is reported. A bicyclic bridgehead phosphoramidite (briphos) ligand together with Pd(dba)2 is a highly efficient catalyst, and an acid additive involved in the rate-determining step promotes the catalytic cycle. The coupling reaction of allylic alcohols with N-heterocycles including imidazoles, benzimidazoles, and triazole proceeds under mild reaction conditions with high yields using Pd/briphos and pentafluorophenol.

Chemokine receptor binding heterocyclic compounds with enhanced efficacy

-

, (2008/06/13)

The invention relates to heterocyclic compounds consisting of a core nitrogen atom surrounded by three pendant groups, wherein two of the three pendant groups are preferably benzimidazolyl methyl and tetrahydroquinolyl, and the third pendant group contains N and optionally contains additional rings. The compounds bind to chemokine receptors, including CXCR4 and CCR5, and demonstrate protective effects against infection of target cells by a human immunodeficiency virus (HIV).

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 6307-15-9