Welcome to LookChem.com Sign In|Join Free

CAS

  • or

858232-97-0

Post Buying Request

858232-97-0 Suppliers

Recommended suppliersmore

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

858232-97-0 Usage

Description

(7-methyl-1H-indol-3-yl)acetonitrile is a chemical compound with the molecular formula C11H10N2, derived from the heterocyclic compound indole, which is commonly found in certain plants and utilized in the synthesis of various pharmaceuticals and organic compounds. (7-methyl-1H-indol-3-yl)acetonitrile features a nitrile functional group, making it a versatile building block for constructing more complex molecules in organic synthesis. The presence of the indole ring and the acetonitrile group endows it with potential applications in medicinal chemistry and other areas within organic chemistry. The 7-methyl substitution on the indole ring may also confer specific properties or reactivity to this compound.

Uses

Used in Pharmaceutical Synthesis:
(7-methyl-1H-indol-3-yl)acetonitrile is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be a versatile building block in creating complex molecules.
Used in Organic Chemistry:
(7-methyl-1H-indol-3-yl)acetonitrile is used as a reagent in organic chemistry due to its nitrile functional group, which allows for further reactions and the formation of a wide range of organic compounds.
Used in Medicinal Chemistry:
(7-methyl-1H-indol-3-yl)acetonitrile is used as a starting material for the development of new drugs in medicinal chemistry, taking advantage of its indole ring and potential for specific reactivity due to the 7-methyl substitution.
Used in Chemical Research:
(7-methyl-1H-indol-3-yl)acetonitrile is used as a research compound to study the properties and reactivity of indole derivatives and nitrile-containing compounds, contributing to the advancement of chemical knowledge and potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 858232-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,2,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 858232-97:
(8*8)+(7*5)+(6*8)+(5*2)+(4*3)+(3*2)+(2*9)+(1*7)=200
200 % 10 = 0
So 858232-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2/c1-8-3-2-4-10-9(5-6-12)7-13-11(8)10/h2-4,7,13H,5H2,1H3

858232-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-METHYLINDOLE-3-ACETONITRILE

1.2 Other means of identification

Product number -
Other names (7-methyl-1H-indol-2-yl)(phenyl)methanone

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:858232-97-0 SDS

858232-97-0Downstream Products

858232-97-0Relevant articles and documents

Tryptamine Synthesis by Iron Porphyrin Catalyzed C?H Functionalization of Indoles with Diazoacetonitrile

Hock, Katharina J.,Knorrscheidt, Anja,Hommelsheim, Renè,Ho, Junming,Weissenborn, Martin J.,Koenigs, Rene M.

supporting information, p. 3630 - 3634 (2019/02/13)

The functionalization of C?H bonds with non-precious metal catalysts is an important research area for the development of efficient and sustainable processes. Herein, we describe the development of iron porphyrin catalyzed reactions of diazoacetonitrile with N-heterocycles yielding important precursors of tryptamines, along with experimental mechanistic studies and proof-of-concept studies of an enzymatic process with YfeX enzyme. By using readily available FeTPPCl, we achieved the highly efficient C?H functionalization of indole and indazole heterocycles. These transformations feature mild reaction conditions, excellent yields with broad functional group tolerance, can be conducted on gram scale, and thus provide a unique streamlined access to tryptamines.

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 858232-97-0