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1,2-Pentadecadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

596815-62-2

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596815-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596815-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,8,1 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 596815-62:
(8*5)+(7*9)+(6*6)+(5*8)+(4*1)+(3*5)+(2*6)+(1*2)=212
212 % 10 = 2
So 596815-62-2 is a valid CAS Registry Number.

596815-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name pentadeca-1,2-diene

1.2 Other means of identification

Product number -
Other names Pentadeca-1,2-dien

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:596815-62-2 SDS

596815-62-2Relevant academic research and scientific papers

Copper(ii)-catalyzed protoboration of allenes in aqueous media and open air

Nekvinda, Jan,Santos, Webster L.,Snead, Russell F.

, p. 14925 - 14931 (2021)

A method has been developed for the facile Cu(ii)-catalyzed protoboration of monosubstituted allenes in aqueous media under atmospheric conditions. The reaction occurs site selectively, favoring internal alkene protoboration to afford 1,1-disubstituted vinylboronic acid derivatives (up to 93?:?7) with modest to good yields. The method has been applied to a variety of phenylallene derivatives as well as alkyl-substituted allenes. This journal is

Highly regio- and stereoselective synthesis of alkylidenecyclopropanes via Ru(II)-pheox catalyzed asymmetric inter- and intramolecular cyclopropanation of allenes

Chanthamath, Soda,Chua, Hao Wei,Kimura, Seiya,Shibatomi, Kazutaka,Iwasa, Seiji

supporting information, p. 3408 - 3411 (2014/07/08)

An efficient protocol for the synthesis of optically active alkylidenecyclopropanes (ACPs) via the Ru(II)-Pheox catalyzed asymmetric cyclopropanation of allenes has been established. This catalytic system proceeded with high regioselectivity to give the A

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