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158426-76-7

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158426-76-7 Usage

Chemical class

Belongs to the cycloalkenes class of organic compounds.

Functional group

Contains a carboxylic acid functional group.

Application

Commonly used as a ligand in transition metal-catalyzed reactions.

Metal complex formation

Known for its ability to form stable complexes with metals, making it versatile in organometallic chemistry.

Structure

Characterized by an eight-carbon ring with a carboxyl group attached at position 1.

Reactivity

Double bonds provide significant reactivity and utility in various chemical reactions.

Importance

Widely used and considered an important chemical in the fields of organic and inorganic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 158426-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,4,2 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158426-76:
(8*1)+(7*5)+(6*8)+(5*4)+(4*2)+(3*6)+(2*7)+(1*6)=157
157 % 10 = 7
So 158426-76-7 is a valid CAS Registry Number.

158426-76-7SDS

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 cycloocta-1,7-diene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,7-CYCLOOCTADIENE-1-CARBOXYLICACID

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:158426-76-7 SDS

158426-76-7Upstream product

158426-76-7Downstream Products

158426-76-7Relevant articles and documents

Asymmetric synthesis of (1S,2R)-2-aminocyclooctanecarboxylic acid

Garrido, Narciso M.,Blanco, Magda,Cascon, Imanol F.,Diez, David,Vicente, Victor M.,Sanz, Francisca,Urones, Julio G.

experimental part, p. 2895 - 2900 (2009/07/11)

A highly efficient asymmetric synthesis of (1S,2R)-2-aminocyclooctanecarboxylic acid has been completed. This asymmetric synthesis using cycloocta-1,5-diene as the starting material is achieved in 77% yield via a four-step sequence from tert-butyl cycloocta-1,7-dienecarboxylate 10 where the extra double bond adjacent to the unsaturated ester is essential to improve the yield. Furthermore, the Michael adduct intermediate (1S,2R,αR)-14 could be used towards the synthesis of the natural product tashiromine.

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