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29493-00-3

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29493-00-3 Usage

Synthesis Reference(s)

Tetrahedron, 44, p. 2875, 1988 DOI: 10.1016/S0040-4020(88)90023-3Tetrahedron Letters, 31, p. 365, 1990 DOI: 10.1016/S0040-4039(00)94556-8

Check Digit Verification of cas no

The CAS Registry Mumber 29493-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,9 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29493-00:
(7*2)+(6*9)+(5*4)+(4*9)+(3*3)+(2*0)+(1*0)=133
133 % 10 = 3
So 29493-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H24/c1-3-5-7-9-11-12-10-8-6-4-2/h11-12H,3-10H2,1-2H3

29493-00-3SDS

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 dodec-6-ene

1.2 Other means of identification

Product number -
Other names Dodec-6-en

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:29493-00-3 SDS

29493-00-3Relevant articles and documents

Synthesis of bio-based monomer from vegetable oil fatty acids and design of functionalized greener polyester

Abd. Rahim, Noor Farisha,Ariffin, Hidayah,Hassan, Mohd Ali,Watanabe, Kohtaro,Andou, Yoshito,Shirai, Yoshihito

, p. 1517 - 1519 (2014)

In order to design sustainable materials from vegetable oilbased fatty acids, we propose herewith a method to obtain unsaturated dicarboxylic acids as a polymerizable monomer through metathesis reaction of oleic and linoleic acids with the 2nd generation Grubbs catalyst. Subsequently, functional green polyester was produced from dicarboxylic acids and aromatic diol. Dicarboxylic acid having similar structure i.e., octadec-9-enedioic acid was successfully obtained from metathesis of both oleic and linoleic acids. Condensation polymerization of octadec-9-enedioic acid with 1,6-hexanediol and 4,4′-biphenol was carried out and it was shown that polymer with aromatic backbone had higher glass-transition temperature than aliphatic polyester.

Transition metal complexes of a bis(carbene) ligand featuring 1,2,4-triazolin-5-ylidene donors: structural diversity and catalytic applications

Donthireddy, S. N. R.,Illam, Praseetha Mathoor,Rit, Arnab,Singh, Vivek Kumar

, p. 11958 - 11970 (2020/09/21)

Dialkylation of the 1,3-bis(1,2,4-triazol-1-yl)benzene with ethyl bromide results in the formation of [L-H2]Br2which, upon salt metathesis with NH4PF6, readily yields the bis(triazolium) salt [L-H2](PF6)2with non-coordinating counterions. [L-H2](PF6)2and Ag2O react in a 1?:?1 ratio to yield a binuclear AgI-tetracarbene complex of the composition [(L)2Ag2](PF6)2which undergoes a facile transmetalation reaction with [Cu(SMe2)Br] to deliver the corresponding CuI-NHC complex [(L)2Cu2](PF6)2. In contrast, the [L-H2]Br2reacts with [Ir(Cp*)Cl2]2to generate a doubly C-H activated IrIII-NHC complex5. Similarly, the triazolinylidene donor supported diorthometalated RuII-complex6is also obtained. Complexes5and6represent the first examples of a stable diorthometalated binuclear IrIII/RuII-complex supported by 1,2,4-triazolin-5-ylidene donors. The synthesized IrIII-NHC complex5is found to be more effective than its RuII-analogue (6) for the reduction of a range of alkenes/alkynesviathe transfer hydrogenation strategy. Conversely, RuII-complex6is identified as an efficient catalyst (0.01 mol% loading) for the β-alkylation of a wide range of secondary alcohols using primary alcohols as alkylating partnersviaa borrowing hydrogen strategy.

Co-metathesis of ethylene and olefinic compounds in ionic liquids

Greish, Alexander A.,Kustov, Leonid M.,Vasnev, Alexander V.

experimental part, p. 329 - 330 (2012/02/01)

Tungsten(VI) chloride dissolved in the ionic liquids is capable of catalyzing metathesis of 4-octene and co-metathesis of 4-penten-1-ol with ethylene; the latter reaction is preceded by double bond shift in the starting alkenol.

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