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97259-61-5

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97259-61-5 Usage

Chemical class

Pyridine

Uses

Synthesis of pharmaceuticals, agrochemicals, flavors, and fragrances

Physical properties

Volatile organic compound with a strong odor

Health hazards

Irritation to respiratory system and skin; handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 97259-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,5 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97259-61:
(7*9)+(6*7)+(5*2)+(4*5)+(3*9)+(2*6)+(1*1)=175
175 % 10 = 5
So 97259-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N/c1-3-8(2)9-6-4-5-7-10-9/h4-7H,2-3H2,1H3

97259-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-but-1-en-2-ylpyridine

1.2 Other means of identification

Product number -
Other names EINECS 306-422-4

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:97259-61-5 SDS

97259-61-5Downstream Products

97259-61-5Relevant articles and documents

Manganese-Catalyzed Direct Nucleophilic C(sp2)-H Addition to Aldehydes and Nitriles

Zhou, Bingwei,Hu, Yuanyuan,Wang, Congyang

supporting information, p. 13659 - 13663 (2015/11/16)

Herein, a manganese-catalyzed nucleophilic addition of inert C(sp2)-H bonds to aldehydes and nitriles is disclosed by virtue of a dual activation strategy. The reactions feature mild reaction conditions, excellent regio- and stereoselectivity, and a wide substrate scope, which includes both aromatic and olefinic C-H bonds, as well as a large variety of aldehydes and nitriles. Moreover, mechanistic studies shed light on possible catalytic cycles.

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