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74205-10-0

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74205-10-0 Usage

Molecular Weight

185.22 g/mol

Physical State

Colorless solid

Usage

Organic synthesis and pharmaceutical research

Role

Important building block in the production of various pharmaceuticals and fine chemicals

Reactivity

High reactivity

Potential

Discovering new drugs

Biological Activities

Studied for anti-inflammatory and anti-cancer properties

Check Digit Verification of cas no

The CAS Registry Mumber 74205-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74205-10:
(7*7)+(6*4)+(5*2)+(4*0)+(3*5)+(2*1)+(1*0)=100
100 % 10 = 0
So 74205-10-0 is a valid CAS Registry Number.

74205-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methoxyphenyl)cyclobutane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:74205-10-0 SDS

74205-10-0Relevant articles and documents

Preparation of Indolenines via Nucleophilic Aromatic Substitution

Huber, Florian,Roesslein, Joel,Gademann, Karl

supporting information, p. 2560 - 2564 (2019/03/19)

An unusual aromatic substitution to access indolenines is described. 2-(2-Methoxyphenyl)acetonitrile derivatives are reacted with various alkyl and aryl Li reagents to furnish the corresponding indolenine products, constituents of natural products, and cyanine dyes such as indocyanine green. This new method was used to synthesize 41 indolenines with large functional group tolerance, and selected examples were further converted to the corresponding indolenine dyes. Key experiments provide insight into the mechanism of this nucleophilic aromatic substitution.

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