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1124-79-4

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1124-79-4 Usage

General Description

(1Z,6Z)-1,6-Cyclodecadiene is a chemical compound with the molecular formula C10H16. It is a cyclic diene, meaning it contains two double bonds within a 10-carbon ring structure. The compound is a colorless liquid at room temperature and is commonly used as a synthetic intermediate in organic chemistry. (1Z,6Z)-1,6-Cyclodecadiene is an important building block for the production of various chemical products, including pharmaceuticals, fragrances, and polymers. It is also used as a starting material for the synthesis of other cyclic compounds and complex organic molecules. The compound is flammable and should be handled and stored with care in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 1124-79-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1124-79:
(6*1)+(5*1)+(4*2)+(3*4)+(2*7)+(1*9)=54
54 % 10 = 4
So 1124-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-2-4-6-8-10-9-7-5-3-1/h1-2,9-10H,3-8H2/b2-1-,10-9-

1124-79-4SDS

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 (1Z,6Z)-cyclodeca-1,6-diene

1.2 Other means of identification

Product number -
Other names cis-1,6-cyclodecadiene

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:1124-79-4 SDS

1124-79-4Upstream product

1124-79-4Relevant articles and documents

Simple Designs for the Construction of Complex Trans-Fused Polyether Toxin Frameworks. A Linear Strategy Based on Entropically Favored Oxirane Ring Enlargement in Epoxycycloalkenes Followed by Carbon-Carbon or Carbon-Oxygen Bond-Forming Cyclizations

Alvarez, Eleuterio,Diaz, Maria T.,Perez, Ricardo,Ravelo, Jose L.,Regueiro, Alicia,et al.

, p. 2848 - 2876 (2007/10/02)

A successful design for the construction of trans-fused medium-size cyclic ethers is described.The key features of the synthesis are as follows: (i) intramolecular oxirane ring expansion in cycloalkenes to give bridged oxabicyclic systems and (ii) linear, one- or two-directional synthetic operations which generate external oxocycles in single reaction steps.The general approach involves the intramolecular addition of a stable γ-alkoxy-substituted allylstannane to an aldehyde carbonyl group, and the entire reaction is conducted in a one-pot process which includes the following: (i) vic-diol fragmentation from the bridged oxabicyclic precursor and (ii) Lewis acid-induced cyclization of the resulting aldehyde-allylic tin system.While the present strategy was mostly developed around racemic models, the potential for adoption of enantioselective features is immediate.The versatility, scope, limitations, and potential applications of the present technology are discussed in detail.

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